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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.
19 In this randomized, blinded, parallel-group, placebo-controlled trial, 150 subjects (age 67 +/- 9 yea
23 his single-centre, randomised, double blind, placebo-controlled trial, 31 patients with aSAH were ran
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
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
43 e, randomised, double-blind, parallel-group, placebo-controlled trial at Glenfield Hospital (Leiceste
45 y cohort, we did a double-blind, randomised, placebo-controlled trial based in Doneguebougou and surr
48 med our study as a randomized, double-blind, placebo-controlled trial by training other subjects in a
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
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
64 uction Trial was a randomized, double-blind, placebo-controlled trial conducted in 3 centers across t
66 se 3, multicenter, randomized, double-blind, placebo-controlled trial conducted in 720 hospitals in 2
69 h Malaria) was a randomized, double-blinded, placebo-controlled trial conducted in malaria-endemic Ug
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
74 Two international, randomized, double-blind, placebo-controlled trials (DUAL-1, DUAL-2) were conducte
81 is highlights the need for more high-quality placebo-controlled trials, equipoise may no longer be gu
83 ntically designed, randomized, double-blind, placebo-controlled trials evaluated the efficacy of bude
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
91 Pooled data from randomized, double-blind, placebo-controlled trials for the clinical development p
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
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
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
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
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
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
121 a challenge to design rigorous, randomized, placebo-controlled trials, in part owing to problems of
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
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
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
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
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
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
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
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
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
186 This was a multisite randomized double-blind placebo-controlled trial of ultra-low-dose sublingual bu
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
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
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-
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
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
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
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
230 to corticosteroids in COPD in a randomized, placebo-controlled trial, the Groningen and Leiden Unive
235 ed a multicenter, double-masked, randomized, placebo-controlled trial to determine the efficacy and s
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
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
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
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
252 ase 2 randomized, multicenter, double-blind, placebo-controlled trial using a sequential parallel com
257 This phase 2, randomised, double-blind, placebo-controlled trial was done in 72 baranguays (vill
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
278 ntre phase 1b, first-in-human, single-blind, placebo-controlled trial, we randomly assigned (1:1) hea
282 n this phase III, multicenter, double-blind, placebo-controlled trial, we randomly assigned patients
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
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
298 KCC) trial was a randomized, double-blinded, placebo-controlled trial with patients from dermatology
300 quantified by comparing simulated randomised placebo-controlled trials within the out-of-sample LABS-
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