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1  reduce symptoms of patients in a randomized placebo-controlled trial.
2 cteristics of CTS in women taking an AI in a placebo-controlled trial.
3                     This was a double-blind, placebo-controlled trial.
4 RISA) 004 study, a double-blind, randomized, placebo-controlled trial.
5  recruited into this double-blind randomized placebo-controlled trial.
6  was reported in a double-blind, randomized, placebo-controlled trial.
7  has not been substantiated by a randomised, placebo-controlled trial.
8 hy, we conducted a randomized, double-blind, placebo-controlled trial.
9  were randomly assigned in a double-blinded, placebo-controlled trial.
10  a multicenter, randomized (1:1 allocation), placebo-controlled trial.
11  a pre-registered, randomised, double-blind, placebo-controlled trial.
12 y.This study was a randomized, double-blind, placebo-controlled trial.
13 presentation in a prospective, double blind, placebo-controlled trial.
14  evaluated in two multicenter, double-blind, placebo-controlled trials.
15         We did two randomised, double-blind, placebo-controlled trials.
16 ally affect interpretation of the results of placebo-controlled trials.
17 umab may be examined in larger double-blind, placebo-controlled trials.
18                        In this double-blind, placebo-controlled trial, 120 asymptomatic Plasmodium fa
19 In this randomized, blinded, parallel-group, placebo-controlled trial, 150 subjects (age 67 +/- 9 yea
20            In this randomized, double-blind, placebo-controlled trial, 18- to 50-year-olds received 2
21                In a randomised double-blind, placebo controlled trial, 22 early onset PD patients, we
22                            We identified 252 placebo-controlled trials (26 324 patients on placebo) d
23 his single-centre, randomised, double blind, placebo-controlled trial, 31 patients with aSAH were ran
24               In a randomised, double-blind, placebo-controlled trial, 40 HIV-infected participants w
25        In this 2 x 2 factorial, double-blind placebo-controlled trial, 457 lead-exposed Moroccan chil
26            In this randomized, double-blind, placebo-controlled trial, 50 patients with biopsy-proven
27  In a multicenter, double-blind, randomized, placebo-controlled trial, 62 patients were allocated to
28 tive, multicenter, randomized, double-blind, placebo-controlled trial, 96 HT recipients were randomiz
29 is international, multicentre, double-blind, placebo-controlled trial, adult patients (>/=18 years) w
30 his single-centre, randomised, double-blind, placebo-controlled trial, adult patients (aged 18 years
31  this multicentre, randomised, double-blind, placebo-controlled trial, adults (>/=18 years) with S au
32                          In this randomized, placebo-controlled trial, adults with newly diagnosed or
33            In this randomised, double-blind, placebo-controlled trial, adults with prediabetes and a
34 ducted a 2-year, randomized, double-blinded, placebo-controlled trial among 2727 households in 3 nort
35 herpes zoster in a randomized, double-blind, placebo-controlled trial among 3408 persons coinfected w
36 tland Coronary Prevention Study) randomized, placebo-controlled trial, and observational posttrial lo
37 s a multi-centric, double-blind, randomized, placebo- controlled trial applying two single doses of O
38  This exploratory, randomized, double-blind, placebo-controlled trial assessed a preemptive antifunga
39               This randomized, double-blind, placebo-controlled trial assessed the effects of tenapan
40      We did this randomised, parallel-group, placebo-controlled trial at 46 secondary care centres in
41            In this randomised, double-blind, placebo-controlled trial at 590 sites in 42 countries, w
42                              Double-blinded, placebo-controlled trial at 9 academic medical centers i
43 e, randomised, double-blind, parallel-group, placebo-controlled trial at Glenfield Hospital (Leiceste
44           We did a randomised, double-blind, placebo-controlled trial at three centres in the USA and
45 y cohort, we did a double-blind, randomised, placebo-controlled trial based in Doneguebougou and surr
46        We did this randomised, double-blind, placebo-controlled trial between Dec 15, 2009, and Oct 2
47            In this randomised, double-blind, placebo-controlled trial, boys from three centres in the
48 med our study as a randomized, double-blind, placebo-controlled trial by training other subjects in a
49                                       In the placebo-controlled trial, clinical remission was defined
50              This multicenter, double-blind, placebo-controlled trial compared the effects of intrave
51 et Therapy Study, a randomized double-blind, placebo-controlled trial, compared 30 versus 12 months o
52 ODS AND TIME was a randomized, double-blind, placebo-controlled trial comparing 150 million bone marr
53   We conducted a double-blinded, randomized, placebo-controlled trial comparing daily TMP-SMX plus mo
54 al, multicenter, randomized, double-blinded, placebo-controlled trial comparing extended (30-months)
55 re included in the randomized, double-blind, placebo-controlled trial, comprising 3 years of treatmen
56  participants in a randomized, double-blind, placebo-controlled trial conducted at 11 clinical center
57           Phase 3, randomized, double-blind, placebo-controlled trial conducted at 18 sites in 12 cou
58 k, randomized, double-blind, parallel-group, placebo-controlled trial conducted at three academic med
59  this prospective, double-blind, randomized, placebo-controlled trial conducted at two tertiary care
60                    Double-blind, randomized, placebo-controlled trial conducted between August 2011 a
61       Multicenter, randomized, double-blind, placebo-controlled trial conducted between May 2010 and
62                           In a double-blind, placebo-controlled trial conducted from 1998 through 200
63                    Randomized, double-blind, placebo-controlled trial conducted in 13 French cardiac
64 uction Trial was a randomized, double-blind, placebo-controlled trial conducted in 3 centers across t
65       Multicenter, randomized, double-blind, placebo-controlled trial conducted in 3 Spanish teaching
66 se 3, multicenter, randomized, double-blind, placebo-controlled trial conducted in 720 hospitals in 2
67               In a randomized, double-blind, placebo-controlled trial conducted in Europe, we assigne
68        A randomized, double-blind, multisite placebo-controlled trial conducted in human subjects dem
69 h Malaria) was a randomized, double-blinded, placebo-controlled trial conducted in malaria-endemic Ug
70                                   Randomized placebo-controlled trial conducted October 2011 through
71 R criteria were enrolled in this randomized, placebo-controlled trial consisting of an initial 12- to
72 ed case-control study and a small randomized placebo-controlled trial demonstrating beneficial effect
73 t 1 consisted of a randomised, double-blind, placebo-controlled trial done over 18 months.
74 Two international, randomized, double-blind, placebo-controlled trials (DUAL-1, DUAL-2) were conducte
75                  A randomized, double-blind, placebo-controlled trial (Effects of Psychotropic Drugs
76      For this phase 3, parallel, randomised, placebo-controlled trial, eligible patients were adults
77      In this first randomized, double-blind, placebo-controlled trial, enoxaparin (40 mg once daily)
78                  Randomized, double-blinded, placebo-controlled trial enrolled 31 patients with recur
79      METHODS AND Randomized, double-blinded, placebo-controlled trial enrolled 31 patients with recur
80                    Double-blind, randomized, placebo-controlled trial, enrolling 92 participants with
81 is highlights the need for more high-quality placebo-controlled trials, equipoise may no longer be gu
82                                           30 placebo-controlled trials evaluated epidural corticoster
83 ntically designed, randomized, double-blind, placebo-controlled trials evaluated the efficacy of bude
84             Methods In the MAP.3 randomized, placebo-controlled trial evaluating exemestane, particip
85                 This is the first randomized placebo-controlled trial evaluating the novel coadminist
86                We identified all randomized, placebo-controlled trials evaluating fluconazole prophyl
87   The authors searched PubMed for randomized placebo-controlled trials examining the efficacy of SSRI
88  conducted a 16-week randomized double-blind placebo-controlled trial for geriatric depression in 143
89  was a multicentre, double-blind, randomised placebo-controlled trial for which patients were recruit
90                                              Placebo-controlled trials for cognitive impairment assoc
91   Pooled data from randomized, double-blind, placebo-controlled trials for the clinical development p
92                                  Randomized, placebo-controlled trial from July 2014 to May 2016.
93 ncluding drug tapers, drug-free periods, and placebo-controlled trials, had a low risk of symptom exa
94 ntraocular pressure, but to our knowledge no placebo-controlled trials have assessed visual function
95  are observational although some randomised, placebo-controlled trials have been conducted with omega
96 e used routinely to treat depression, yet no placebo-controlled trials have been published in this po
97                                   Randomised placebo-controlled trials have shown that daily oral pre
98 ollowing up these findings in a double-blind placebo controlled trial in nondiabetic heart failure (t
99 nducted a phase 2, randomized, double-blind, placebo-controlled trial in 27 centers across North Amer
100  We undertook this randomised, double-blind, placebo-controlled trial in a general adult intensive ca
101        We did this randomised, double-blind, placebo-controlled trial in antenatal clinics at 15 Nati
102        In a previously described randomised, placebo-controlled trial in Dhaka, Bangladesh, we showed
103         We did this multicentre, randomised, placebo-controlled trial in four centres in Kenya.
104                                Double-blind, placebo-controlled trial in HIV+ with CD4(+) T cells/mic
105 terventions, describe evidence from a recent placebo-controlled trial in India suggesting that contro
106 onducted a cluster-randomized, double-blind, placebo-controlled trial in Indonesia and assigned 954 h
107                   We conducted a randomized, placebo-controlled trial in Niger to evaluate the effica
108                           In a double-blind, placebo-controlled trial in Niger, we randomly assigned
109 udy consisted of a randomised, double-blind, placebo-controlled trial in patients with IPF and chroni
110 hase 2 double-blind, multicentre, randomised placebo-controlled trial in previously untreated adult p
111 ased, individually randomised, double-blind, placebo-controlled trial in the Brong Ahafo region of Gh
112        We did this randomised, double-blind, placebo-controlled trial in two tertiary-care hospitals
113 ydants study was a randomized, double-blind, placebo-controlled trial in which participants received
114 ed a multi-center, double-blind, randomized, placebo-controlled trial in which smokers hospitalized w
115     We performed a randomized, double-blind, placebo-controlled trial in which, after perioperative i
116      We report two double-blind, randomised, placebo-controlled trials in adults with chronic non-can
117                                              Placebo-controlled trials in drug-free patients have lon
118   The authors present a meta-analysis of all placebo-controlled trials in patients with acute exacerb
119 onducted to identify double-blind randomized placebo-controlled trials in schizophrenia or related di
120                We reanalyzed 2 double-blind, placebo-controlled trials in unmedicated middle-aged men
121  a challenge to design rigorous, randomized, placebo-controlled trials, in part owing to problems of
122                             This randomized, placebo-controlled trial included 4- to 6-month-old infa
123 THOD: This 6-week, randomized, double-blind, placebo-controlled trial included patients with schizoph
124 Trial (CAST) was a randomized, double-blind, placebo-controlled trial involving 201 patients with sta
125     We conducted a randomized, double-blind, placebo-controlled trial involving 27,564 patients with
126     We conducted a randomized, double-blind, placebo-controlled trial involving 30,449 adults with at
127               In a randomized, double-blind, placebo-controlled trial involving 84,496 adults 65 year
128     We performed a randomized, double-blind, placebo-controlled trial involving human immunodeficienc
129 ted a multicenter, randomized, double-blind, placebo-controlled trial involving patients in whom peri
130 metabolic alkalosis, but no large randomized placebo-controlled trial is available to confirm this ap
131                                           No placebo-controlled trials met inclusion criteria, eviden
132 week, prospective, double-blind, randomized, placebo-controlled trial (methylphenidate versus placebo
133 undertook a phase I double-blind, randomized placebo controlled trial of vaccination with AERAS-402 f
134 re search in MEDLNE and included randomized, placebo controlled trials of RAAS inhibitors in chronic
135  We performed a single-center, double-blind, placebo-controlled trial of 2 separate cohorts (March 20
136    We performed a prospective, double-blind, placebo-controlled trial of 449 consecutive patients und
137 s), we performed a randomized, double-blind, placebo-controlled trial of 5 days of 80 mg lovastatin v
138 gle site, we did a randomised, double-blind, placebo-controlled trial of a monovalent influenza A H1N
139 nducted a phase 3, randomized, double-blind, placebo-controlled trial of a monthly vaginal ring conta
140  a double-blind, randomized, parallel-group, placebo-controlled trial of a single ketamine infusion (
141 n ongoing phase 2, randomised, double-blind, placebo-controlled trial of a TDV is being done at three
142 e, double-blind, randomised, parallel-group, placebo-controlled trial of A1PI treatment in patients w
143 med a prospective, randomized, double-blind, placebo-controlled trial of adults with eosinophilic eso
144     We conducted a randomized, double-blind, placebo-controlled trial of amitriptyline (1 mg per kilo
145 nine ratios; 443 were randomly assigned in a placebo-controlled trial of an ACE inhibitor and a stati
146 rollment within the context of a randomized, placebo-controlled trial of an investigational agent for
147 e of exception from informed consent in this placebo-controlled trial of an investigational agent was
148 ere we report on a randomized, double-blind, placebo-controlled trial of an oral synbiotic preparatio
149     We performed a randomized, double-blind, placebo-controlled trial of anastrozole in patients with
150  the Physicians' Health Study, a randomized, placebo-controlled trial of aspirin and beta-carotene am
151 G) participated in a randomised double-blind placebo-controlled trial of blood- plus liver-stage drug
152           We did a randomised, double-blind, placebo-controlled trial of canakinumab in 10 061 patien
153 lled in a randomized, 3-month double-masked, placebo-controlled trial of daily 2 g DHA or placebo cap
154 ata from women in the Partners PrEP Study, a placebo-controlled trial of daily oral PrEP (either teno
155 is of the Partners PrEP Study, a randomized, placebo-controlled trial of daily oral TDF, alone or wit
156     We performed a randomized, double-blind, placebo-controlled trial of DAR-0100A (15 mg/150 ml of n
157 MDD patients enrolled in a large, randomized placebo-controlled trial of duloxetine collected before
158 tients with UC who participated in a phase 2 placebo-controlled trial of etrolizumab, as well as from
159 In a subgroup of patients from a randomized, placebo-controlled trial of evolocumab added to statin t
160             We performed a proof of concept, placebo-controlled trial of extended-release phentermine
161 bstudy of iPrEx, a randomized, double-blind, placebo-controlled trial of FTC/TDF PrEP.
162 (ViDA) Study was a randomised, double-blind, placebo-controlled trial of healthy volunteers aged 50-8
163 arting antiretroviral therapy (ART) during a placebo-controlled trial of HSV-2 suppression with acycl
164 Healthy adults participating in a randomized placebo-controlled trial of inactivated (IIV) and live-a
165 t participants (age range, 18-49 years) in a placebo-controlled trial of inactivated influenza vaccin
166 id an individually randomised, double-blind, placebo-controlled trial of infants born in the Morogoro
167 MAGiC) study was a randomized, double-blind, placebo-controlled trial of intravenous magnesium vs nor
168                        No large, randomized, placebo-controlled trial of iodine supplementation in pr
169                                   Randomised placebo-controlled trial of low-dose and high-dose fish
170 ngs from a 12-week randomized double-blinded placebo-controlled trial of methylphenidate or galantami
171     We conducted a double-blind, randomized, placebo-controlled trial of MMS in 17- to 45-y-old Gambi
172 ible for a nested, randomised, double-blind, placebo-controlled trial of MVA-BN-Filo.
173 t baseline and multiple time points during a placebo-controlled trial of OIT for milk allergy in whic
174      In this first randomized, double-blind, placebo-controlled trial of omalizumab in combination wi
175 rteen-week, randomized, double-blind, 3-arm, placebo-controlled trial of participants meeting DSM-IV-
176 n an international, randomized, double-blind placebo-controlled trial of patients with nonalcoholic s
177 aseline and at multiple time points during a placebo-controlled trial of peanut OIT and SLIT.
178 rvention After Stroke trial, a double-blind, placebo-controlled trial of pioglitazone for secondary p
179 e Parents (ECAP) were tested in a randomized placebo-controlled trial of pre-emptive high-dose flutic
180  key psychometric properties in a randomized placebo-controlled trial of pre-emptive high-dose flutic
181 part of a parallel-design, block-randomized, placebo-controlled trial of preconception LDA.
182     We conducted a randomized, double-blind, placebo-controlled trial of pregabalin in patients with
183 ts, we conducted a randomized, double-blind, placebo-controlled trial of supplementation with vitamin
184 n 3381 HIV/HSV-2-coinfected individuals in a placebo-controlled trial of suppressive acyclovir therap
185           We did a double-blind, randomised, placebo-controlled trial of the effect of azithromycin o
186 This was a multisite randomized double-blind placebo-controlled trial of ultra-low-dose sublingual bu
187           We did a double-blind, randomised, placebo-controlled trial of vaginal progesterone, 200 mg
188                   We conducted a randomized, placebo-controlled trial of valganciclovir therapy in ne
189 re enrolled in a randomized, double-blinded, placebo-controlled trial of vitamin D supplementation du
190 l-conducted large, randomized, double-blind, placebo-controlled trial of vitamin D supplementation fo
191           We did a randomised, double-blind, placebo-controlled trial of vitamin D3 supplementation i
192 s P-TIMI 50) was a randomized, double-blind, placebo-controlled trial of vorapaxar in 26,449 patients
193 IMI 50 trial was a randomized, double-blind, placebo-controlled trial of vorapaxar in patients with s
194 s P-TIMI 50) was a randomized, double-blind, placebo-controlled trial of vorapaxar in stable patients
195 on 54) (ticagrelor) were blinded, randomized placebo-controlled trials of antiplatelet therapy for th
196 shed and unpublished double-blind randomised placebo-controlled trials of first-generation and second
197 rom two phase III, randomized, double-blind, placebo-controlled trials of IFN-gamma-1b in idiopathic
198 on: Few studies of acute gout treatments, no placebo-controlled trials of management of hyperuricemia
199 his review analyzed randomized double-blind, placebo-controlled trials of molecularly targeted therap
200  Jan 31, 2016, for randomised, double-blind, placebo-controlled trials of second-generation antidepre
201 d two multicenter, randomized, double-blind, placebo-controlled trials of subcutaneous implants conta
202          Data from randomized, double-blind, placebo-controlled trials of Timothy grass SLIT-tablet M
203 ted three phase 3, randomized, double-blind, placebo-controlled trials of tofacitinib therapy in adul
204   We conducted two double-blind, randomized, placebo-controlled trials of trivalent inactivated influ
205 as been clearly demonstrated, a double-blind placebo-controlled trial on the effect of low-molecular-
206              In a multicenter, double-blind, placebo-controlled trial, participants presenting with a
207             In this phase III, double-blind, placebo-controlled trial, patients with chemotherapy-nai
208 Patients and Methods In this double-blinded, placebo-controlled trial, patients with HER2-positive ea
209 his single-centre, randomised, double-blind, placebo-controlled trial, patients with moderate Parkins
210 ture clinical research should focus on large placebo-controlled trials, powered for perinatal outcome
211                          In this randomised, placebo-controlled trial, pregnant women in Bangalore, I
212 nance imaging to a randomized, double-blind, placebo-controlled trial (RCT) of antidepressant medicat
213 Previously, we demonstrated in a randomized, placebo-controlled trial (RCT) that these infections can
214               This randomized, double-blind, placebo-controlled trial recruited patients aged 18 to 7
215               This double-blind, randomised, placebo-controlled trial recruited patients from seven U
216 d even higher protection against HIV than in placebo-controlled trials, refuting concerns that effect
217 ERVE-AMI (Phase 2, randomized, double-blind, placebo-controlled trial) represents the largest study o
218                           In two consecutive placebo-controlled trials (SET and RESET), we assessed s
219  found in all four much smaller, randomized, placebo-controlled trials specifically designed to evalu
220 lth Study II was a randomized, double-blind, placebo-controlled trial testing multivitamin use (multi
221 ept study (POC) was an 8-week, double-blind, placebo-controlled trial that evaluated LY2940094 as a n
222 rial (SCUT) was a randomized, double-masked, placebo-controlled trial that overall found no effect of
223 rapy to Lower Cardiovascular Events trial, a placebo-controlled trial that randomized 3883 hemodialys
224 was a multicenter, double-blind, randomized, placebo-controlled trial that randomly assigned patients
225 essment Study is a randomized, double-blind, placebo-controlled trial that recruited participants mos
226 was a multicentre, double-blind, randomised, placebo-controlled trial that recruited pregnant women f
227       We used a 4-way randomized, crossover, placebo-controlled trial that was balanced for period an
228                          In this randomized, placebo-controlled trial (the Bortezomib in Late Antibod
229               In a randomized, double-blind, placebo-controlled trial (the Dietary Intervention, Stem
230  to corticosteroids in COPD in a randomized, placebo-controlled trial, the Groningen and Leiden Unive
231                   We conducted a randomized, placebo-controlled trial to assess daily treatment with
232                 We conducted a double-blind, placebo-controlled trial to assess the effect of the ext
233               This was a 12-week randomized, placebo-controlled trial to assess the efficacy of queti
234         The authors conducted a double-blind placebo-controlled trial to assess whether high-dose ora
235 ed a multicenter, double-masked, randomized, placebo-controlled trial to determine the efficacy and s
236                    We performed a randomized placebo-controlled trial to determine the long-term effi
237     We performed a randomized, double-blind, placebo-controlled trial to determine whether a combinat
238     We performed a double-blind, randomized, placebo-controlled trial to determine whether co-adminis
239                 We conducted a double-blind, placebo-controlled trial to evaluate the effect of granu
240     We performed a randomized, double-blind, placebo-controlled trial to evaluate the effects of anti
241 ormed a phase IIb, randomized, double-blind, placebo-controlled trial to evaluate the efficacy and sa
242                 We performed a double-blind, placebo-controlled trial to evaluate the efficacy of par
243 rom 1092 patients enrolled in a double-blind placebo-controlled trial to evaluate the efficacy of tre
244     We performed a double-blind, randomized, placebo-controlled trial to examine whether GTCs protect
245 s conducted a 6-week randomized double-blind placebo-controlled trial to investigate the efficacy of
246 ps, we conducted a double-blind, randomized, placebo-controlled trial to investigate whether vitamin
247                 This is the first randomised placebo-controlled trial to show preservation of the vis
248 e is enough equipoise to justify randomized, placebo-controlled trials to determine if nonparaneoplas
249 e is enough equipoise to justify randomized, placebo-controlled trials to determine whether patients
250                  REMOVAL was a double-blind, placebo-controlled trial undertaken at 23 hospital diabe
251                        In this double-blind, placebo-controlled trial, undertaken across three UK Nat
252 ase 2 randomized, multicenter, double-blind, placebo-controlled trial using a sequential parallel com
253 ering B vitamins on brain atrophy rates in a placebo-controlled trial (VITACOG).
254                   A randomized double-blind, placebo-controlled trial was conducted in 1104 healthy s
255                This multicenter, randomized, placebo-controlled trial was conducted in 30 patients wi
256                A double-blinded, randomized, placebo-controlled trial was conducted to assess the nee
257      This phase 2, randomised, double-blind, placebo-controlled trial was done in 72 baranguays (vill
258               This double-blind, randomised, placebo-controlled trial was done in 90 international ce
259                  A randomized, double-blind, placebo-controlled trial was performed in 16 ICUs in sev
260                A randomized, single-blinded, placebo-controlled trial was performed on 25 subjects: 1
261         A phase 3, randomized, double-blind, placebo-controlled trial was performed to evaluate the s
262                   The aim of this randomized placebo-controlled trial was to determine if withdrawing
263                  This phase 3, double-blind, placebo-controlled trial was undertaken at 101 internati
264  This multicentre, randomised, double-blind, placebo-controlled trial was undertaken at 39 sites (mos
265  this multicenter, double-blind, randomized, placebo-controlled trial, we assessed the efficacy and s
266  In a multicenter, randomized, double-blind, placebo-controlled trial, we compared alefacept (two 12-
267   In this phase 2, randomized, double-blind, placebo-controlled trial, we compared subcutaneous tezep
268  In a prospective, randomized, double-blind, placebo-controlled trial, we enrolled patients with atri
269           In this randomised, triple-masked, placebo-controlled trial, we enrolled patients with newl
270           For this double-blind, randomised, placebo-controlled trial, we enrolled self-referred or p
271                 In this phase 4, randomised, placebo-controlled trial, we enrolled two consecutive se
272              In this double-blind randomised placebo-controlled trial, we enrolled undiagnosed patien
273                                         In a placebo-controlled trial, we found that the probiotic BL
274               In a double-blind, randomized, placebo-controlled trial, we investigated the effect of
275            In this randomized, double-blind, placebo-controlled trial, we investigated the effect of
276                  In a phase 2, double-blind, placebo-controlled trial, we randomized 63 nonosteoporot
277            In this randomised, double-blind, placebo-controlled trial, we randomly allocated 172 57 (
278 ntre phase 1b, first-in-human, single-blind, placebo-controlled trial, we randomly assigned (1:1) hea
279                        In this double-blind, placebo-controlled trial, we randomly assigned 120 child
280           In this multicenter, double-blind, placebo-controlled trial, we randomly assigned 1776 wome
281                        In this double-blind, placebo-controlled trial, we randomly assigned 558 hyper
282 n this phase III, multicenter, double-blind, placebo-controlled trial, we randomly assigned patients
283                        In this double-blind, placebo-controlled trial, we randomly assigned pregnant
284            In this double-blind, randomized, placebo-controlled trial, we recruited adult patients wi
285            For this multicentre, randomised, placebo-controlled trial, we recruited adults (aged 18-6
286            In this randomised, double-blind, placebo-controlled trial, we recruited patients aged at
287               In this phase 3, double-blind, placebo-controlled trial, we recruited patients with pro
288   In a double-blind, multicentre, randomised placebo-controlled trial, we recruited women who had bee
289 lot prospective, randomized, double-blinded, placebo-controlled trial, we studied whether 14 days of
290 n a preregistered, randomized, double-blind, placebo-controlled trial, we tested the effect of a sing
291                              Two randomized, placebo-controlled trials were performed with 168 flaviv
292 udy and an integrated analysis based on five placebo-controlled trials were summarized.
293 o determine, in a multicenter double-blinded placebo-controlled trial, whether maximal hepatic arteri
294 study, data were pooled from two randomized, placebo-controlled trials, which were originally designe
295     We performed a randomized, double-blind, placebo-controlled trial with a 12-week baseline period
296               We thus performed a randomized placebo-controlled trial with atorvastatin 40 mg/day for
297        We now report that in a double-blind, placebo-controlled trial with healthy participants, acut
298 KCC) trial was a randomized, double-blinded, placebo-controlled trial with patients from dermatology
299                     This was a double-blind, placebo-controlled trial with subjects randomized to oma
300 quantified by comparing simulated randomised placebo-controlled trials within the out-of-sample LABS-

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