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1 BAAR) in a double-blind, placebo-controlled, crossover study.
2 requency to 12 healthy volunteers in a 2 x 2 crossover study.
3 S were included in a randomised, controlled, crossover study.
4 k, phase 4, randomized, investigator-masked, crossover study.
5  were enrolled in a prospective, randomized, crossover study.
6 separate days in a randomized, double-blind, crossover study.
7 -blind, placebo-controlled, counterbalanced, crossover study.
8 completed this 3-week inpatient, randomized, crossover study.
9 eted this four-centre, double-blind, two-way crossover study.
10             Experiment one is a five-session crossover study.
11 3.7 +/- 3.5 y) were included in a randomized crossover study.
12     Thirty-one surgeons were recruited for a crossover study.
13 rticipated in this randomized, subject-blind crossover study.
14 omized, double-blind, placebo-controlled 3x3 crossover study.
15 corrected, double-blind, placebo-controlled, crossover study.
16 ed, double-blind, placebo-controlled, triple-crossover study.
17 IU) or placebo in a double-blind, randomized crossover study.
18 e studied in this randomized, double-blinded crossover study.
19 in a randomized placebo-controlled three-way crossover study.
20 were enrolled in a 3-period, 7-wk randomized crossover study.
21 ach for 6 weeks in a randomized double-blind crossover study.
22 clonidine, and paroxetine) in a double-blind crossover study.
23 utput in a double-blind, placebo-controlled, crossover study.
24 ) participated in a randomized, double-blind crossover study.
25 icipated in a randomized, placebo-controlled crossover study.
26 andomized, double-blind, placebo-controlled, crossover study.
27 ted in a single-blinded, randomized, 2-phase crossover study.
28 placebo-controlled, randomized, double-blind crossover study.
29 s part of a double-blind, placebo-controlled crossover study.
30 /- 0.6 g/dl) were studied in this randomized crossover study.
31 abetes in a randomized, single-blind, triple-crossover study.
32 -htrA in a double-blind, placebo-controlled, crossover study.
33 (10)]) or air in a double-blind, randomized, crossover study.
34 ram) to placebo in a randomized double-blind crossover study.
35 double blind, placebo-controlled, two-period crossover study.
36  0.5 N saline in a double-blind, randomized, crossover study.
37 hma completed this double-blind, four-period crossover study.
38  consumed on sequential days in a randomized crossover study.
39 sly over 4 hours via pump in this randomized crossover study.
40 obtained through an isotopic double-labeling crossover study.
41 rdia syndrome in a randomized, single-blind, crossover study.
42 a two-drug, placebo-controlled, double-blind crossover study.
43 n; 191.9 +/- 9.9 kcal added) in a randomized crossover study.
44 asked crossover design and 1 with 4 parallel crossover studies.
45          Both were randomized, double-blind, crossover studies.
46 ed in this placebo-controlled, double-blind, crossover study (0.5 mg/kg cortisol or intravenous place
47               In a single-blind, randomized, crossover study, 10 insulin-resistant men consumed 3 hig
48              In a randomized, double-blinded crossover study, 10 overweight or obese volunteers witho
49               In a randomized, double-blind, crossover study, 10 postmenopausal women without additio
50                                 In our human crossover study, 11 healthy subjects were studied under
51                     In a 2-day, double-blind crossover study, 11 lean and 11 obese healthy women unde
52           In this multicenter, double-blind, crossover study, 110 patients with heart failure and a p
53              In a randomized, single-blinded crossover study, 12 healthy white men [mean age: 24 y; B
54 andomized, double-blind, placebo-controlled, crossover study, 12 healthy, young males received gonado
55                              In a randomized crossover study, 13 volunteers consumed fresh and fermen
56             In this double-blind, randomized crossover study, 14 men aged 20-31 y were fed low-zinc a
57                              In a randomized crossover study, 14 patients with OSA attended two sleep
58 genous pathway.In a randomized, double-blind crossover study, 16 healthy individuals were supplemente
59                              In a controlled crossover study, 16 healthy iron-replete volunteers unde
60     In this single-blind, placebo-controlled crossover study, 16 participants completed two study day
61 diet for 100 d) and to human volunteers in a crossover study (180 g/d for 4 d).
62                  In an open-label randomized crossover study, 19 healthy firefighters (age, 41+/-7 ye
63  randomized, double-blind placebo-controlled crossover study, 19 patients with mild-to-moderate idiop
64               In a double-blind, randomized, crossover study, 20 men with prior myocardial infarction
65               In a randomized, double-blind, crossover study, 20 patients with major depression were
66  genotype-stratified, double-blind, four-way crossover study, 21 healthy adult subjects were exposed
67                                      In this crossover study, 3- to 5-y-old children (n = 10 boys, 16
68                                       In the crossover study, 31 healthy volunteers completed two ran
69    In a multicenter, randomized, open-label, crossover study, 34 blacks with stable CAD receiving ace
70                     In this dose-escalating, crossover study, 34 healthy men received a 6-h double-bl
71                       In a randomized, 2-way crossover study, 39 healthy men consumed a meal that con
72 on instructions; (3) an adequately conducted crossover study; (4) comparison of equivalent doses; (5)
73                    In this single-blind case-crossover study, 41 healthy subjects underwent an extens
74       In a double-blind, placebo-controlled, crossover study, 44 elderly subjects were randomly assig
75                                      In this crossover study, 45 male patients with coronary artery d
76  a prospective, single-center, single-blind, crossover study, 56 patients with non-ST-elevation acute
77                       In a blinded, 2-cycle, crossover study, 59 platelet donors were randomized to r
78 acebo-controlled, multiple-dose, 2-sequence, crossover study, 64 patients were randomized to receive
79 s in a randomized, double-blind manner, with crossover studies 7 to 10 days later.
80                This double-blind, randomized crossover study addressed the impact of daily stressors
81 9% predicted) in a double blind, randomized, crossover study after aerosolization of a single dose of
82                     This randomized, blinded crossover study aimed to document if stimulation at 75%
83                                            A crossover study analysis was done on the 259 patients wh
84 on is proposed in detail and is supported by crossover studies and a number of unambiguous experiment
85  time and with published data and the use of crossover studies and adjustment equations to ensure com
86 d, double-blind, placebo-controlled, two-way crossover studies and an open study in nonallergic subje
87 randomized, placebo-controlled, single-blind crossover study and compared with 12 healthy, nonobese c
88 pated in a double-blind, placebo-controlled, crossover study and inhaled single doses of fluticasone
89 s, including Hammett plots, Eyring analysis, crossover studies, and investigations of the influence o
90 used include multiple-arm trials, randomized crossover studies, and more compromised designs such as
91 ional Poisson regression analysis and a case-crossover study approach.
92                         A placebo-controlled crossover study assessed the opioid pharmacodynamic prof
93 ouble-blind, randomised, placebo-controlled, crossover study at 24 sites in North America and Europe.
94 d, double-blind, placebo-controlled 2-period crossover study at 7 neuromuscular referral centers in 4
95 ouble-blind, placebo-controlled, two-period, crossover study at one UK centre.
96 n-label, multicentre, randomised controlled, crossover study between Dec 1, 2012, and Dec 23, 2014, r
97  the meta-analysis was limited to randomized crossover studies, both systolic [1.3 (-0.3, 2.9) mm Hg;
98               This open-label, dose-ranging, crossover study (COMPACT Phase II) was conducted in 18 p
99                                 A randomized crossover study compared the effects of a statin (ceriva
100                 This double-blind randomized crossover study compared the impact of 4 wk of supplemen
101                                Randomized or crossover studies comparing antianginal drugs from 2 or
102 med a randomized, double-blind, single-dose, crossover study comparing 0.5 mg/kg MPH with 1.0 mg/kg A
103 s for bleeding in a prospective, randomized, crossover study comparing 6 months of anti-inhibitor coa
104 rticipated in this randomized, double-blind, crossover study comparing a single dose of NO3-rich beet
105                                   An initial crossover study comparing dual- and single-site right at
106      We performed an open-label, randomized, crossover study comparing overnight closed-loop therapy
107 pen-label, expanded safety and acceptability crossover study comparing rectally applied reduced-glyce
108                   We conducted a randomized, crossover study comparing selective heart rate reduction
109 ans, we performed a randomized, double-blind crossover study comparing the calcium antagonist amlodip
110 double-blind, randomized, placebo-controlled crossover study comparing the effect of the bradykinin B
111 ucted a randomized, multicenter, open-label, crossover study comparing the efficacy and safety of a 1
112 adults underwent a randomized, double-blind, crossover study comparing the vascular response to the 2
113 ion-level exposure time trends can bias case-crossover studies conducted among "first-wave" users of
114 ESIGN, SETTING, AND PARTICIPANTS: Randomized crossover study conducted between January 1 and December
115 zed, controlled, examiner-blind, nine-period crossover study conducted in 72 adult subjects over a 3-
116                                    This case-crossover study, conducted between July 2007 and May 200
117 y-seven patients on hemodialysis completed a crossover study consisting of two exercise training phas
118                              In a randomized crossover study, cynomolgus monkeys were fed either a co
119         A randomized, double-blind, 5-period crossover study design (n = 22) was used to examine the
120               We used a time-stratified case-crossover study design and conditional logistic regressi
121                             We used the case-crossover study design to compare the reported use of ma
122                                       A case-crossover study design was used to analyze ischemic even
123                                       A case-crossover study design was used to investigate associati
124   A randomized, controlled, 3-diet, 3-period crossover study design was used.
125 andomized, controlled three-period (ABB/BAA) crossover study design was used.
126                       A time-stratified case-crossover study design was used.
127                                            A crossover study design was used: the bion was on for the
128             Using a double-blind, randomized crossover study design, 24 healthy volunteers completed
129 nd pacing backup (AAI-30) in a double-blind, crossover study design, followed by an uncontrolled and
130                 Using a time-stratified case-crossover study design, we found a 10.4% change (95% con
131 ing a prospective, randomized, single-blind, crossover study design, we therefore measured EE and rat
132 eve catecholamine depletion in a randomized, crossover study design.
133 ts and ER visits for GI illness using a case-crossover study design.
134 randomized, double-blind, placebo-controlled crossover study design.
135  self-matched control data based on the case-crossover study design.
136 ropriate number of subjects for parallel and crossover study designs.
137                    A prospective, randomized crossover study directly comparing blood culture contami
138 double-blind, placebo-controlled, randomized crossover study, disease-free patients at least 1 year p
139                                         In a crossover study done in medical centres in France, Italy
140 es from 14 mildly hypertensive patients in a crossover study during a high-sodium (HS, 160 mmol/d) di
141 ght adolescents participated in a randomized crossover study during which EAH was measured as intake
142                  Thereafter, in a randomized crossover study, each participant performed a patient-sp
143 e-center, double-masked, placebo-controlled, crossover study evaluated the efficacy of 8 weeks of tre
144  a randomized, double-blind, ascending-dose, crossover study evaluating 3 doses of BG9719 in 63 patie
145 double-blind, randomized, placebo-controlled crossover study evaluating the effect of 14 days of XEN-
146                    Randomized, double-blind, crossover study evaluating twice daily fluticasone propi
147 ed, controlled, examiner-masked, five-period crossover study examined plaque removal in 25 subjects f
148                              This randomized crossover study examined whether EAA supplementation wit
149                   The present within-subject crossover study examines the variability in individual r
150                                 A randomized crossover study explored whether viewing different scene
151                    Extensive double-labeling crossover studies have been conducted.
152                We undertook three randomised crossover studies in 19 patients aged 5-18 years with ty
153           We did a double-blind, randomised, crossover study in 11 patients with asthma and 13 matche
154 randomized, double-blind, placebo-controlled crossover study in 14 nondiabetic overweight or obese (b
155 a randomized double-blind placebo-controlled crossover study in 16 men, with measurement of liver 11b
156 andomized, double-blind, placebo-controlled, crossover study in 21 PD patients on levodopa but no ago
157 randomized, placebo-controlled, four-period, crossover study in 24 patients with T2D, dipeptidyl pept
158 ducted a randomized, double-blind, three-way crossover study in 27 patients with proteinuric CKD to c
159 ouble-blind, randomised, placebo-controlled, crossover study in a hospital and two infirmaries in the
160                              In a randomized crossover study in a metabolic unit, 15 young adults wer
161            This was a prospective randomized crossover study in nonintubated patients with AHRF with
162                          We conducted a case-crossover study in Ontario, Canada between 2004 and 2011
163                   In this blinded, 3-period, crossover study in stable patients with coronary artery
164 attacks by conducting an internet-based case-crossover study in the United States (in 2003-2010) amon
165  75 mg in a 3-period (12 days each) blinded, crossover study in VE (n = 73; mean: 79 +/- 3 years of a
166                        We did a random-order crossover study in volunteers at least 18 years old who
167       We performed a randomized double-blind crossover study in which 32 healthy adults (25.9 +/- 6.6
168 t hoc analysis of the data is functionally a crossover study in which only surviving patients can cro
169 ng men participated in a randomized 3 x 2-wk crossover study in which the following 3 isocaloric diet
170 completed a double-blind, placebo-controlled crossover study in which they received 2 daily subcutane
171                                    This case-crossover study included 27,540 adults with RD from Fren
172 double-blind, randomized, placebo-controlled crossover study included 44 CF patients (aged 7-19 y; 20
173               This double-blind, randomized, crossover study included serial assessments of resting e
174 nalyzed data from 13 double-blind randomized crossover studies including 282 participants (140 health
175                                         Case-crossover studies investigating the association between
176                A 5-year natural experimental crossover study involving patients admitted to four ICUs
177                               We performed a crossover study involving seven totally blind subjects w
178 ouble-blind, randomized, placebo-controlled, crossover study, LSD (200 mug) and placebo were administ
179                                              Crossover studies (m-->F, f-->M) demonstrated that enhan
180                                       In the crossover study, mean removal rate was 94.6% (SD = 6.5%)
181  9), randomized clinical trials (n = 9), and crossover studies (n = 5).
182    DESIGN, SETTING, AND PARTICIPANTS: A case-crossover study nested within a prospective cohort study
183                In a double-blind, randomised crossover study, nine healthy subjects completed knee-ex
184                                      In case-crossover studies of medications, contamination by persi
185 iculate matter (</=2.5 micro m) using a case-crossover study of 1,206 Washington State out-of-hospita
186 e-center, randomized, double-blind, 3-period crossover study of 11 women with IBS (35.50 +/- 12.48 ye
187  new study model, we performed a randomized, crossover study of 12 adult asthmatics who required 800
188   In a single-blinded and placebo-controlled crossover study of 15 healthy participants, we administe
189 EMENTS: In a randomized, placebo-controlled, crossover study of 192 subjects with moderate asthma, we
190 The authors examined this question in a case-crossover study of 20 US cities.
191                       We did a nested cohort crossover study of 28 participants in the PUVA follow-up
192 , AND PARTICIPANTS: Prospective, nested case-crossover study of 288 cases of sudden cardiac death wit
193 age, 62 +/- 7 years) completed a, randomized crossover study of 4 weeks of both low (DSR) and normal
194 e, and substrate metabolism in a prospective crossover study of 4-month duration, consisting of four
195 llen Children and Adolescent study is a case-crossover study of 644 children and adolescents (aged 2-
196 dication and serious fall injuries in a case-crossover study of 90 127 Medicare beneficiaries who wer
197              A pragmatic cluster randomized, crossover study of 9340 patients admitted to 5 adult int
198 andomized, double-blind, placebo-controlled, crossover study of Adderall in 27 well-characterized adu
199                          In this short-term, crossover study of adolescents with newly diagnosed hype
200                       A time-stratified case-crossover study of ambient ozone exposure and emergency
201           A double-blind, placebo-controlled crossover study of caloric deprivation was conduced in a
202 e performed a randomized, placebo-controlled crossover study of CRF compared with saline injection in
203 ble-blinded, randomized, placebo-controlled, crossover study of DBS targeting the ventral striatum/an
204    A randomized, blinded, placebo-controlled crossover study of either 0.5 mg neostigmine or saline (
205          A randomized, open-label, 2-period, crossover study of healthy subjects (n = 160, age 18 to
206 randomized, double-blind, placebo-controlled crossover study of individuals with self-reported non-ce
207 centre, placebo-controlled, double-blind 2x2 crossover study of ivacaftor treatment was conducted in
208 ble-blind, double-dummy, placebo-controlled, crossover study of objectively assessed nonsmokers (n =
209 nd, placebo-controlled, randomized, 3-period crossover study of OPC-28326 (oral doses of 10 mg or 40
210  conducted a multi-site time-stratified case-crossover study of ozone exposures for approximately 3.7
211  44) was a randomized, double-blind, 2-phase crossover study of prasugrel compared with high-dose clo
212                Patients were randomized in a crossover study of pravastatin and simvastatin.
213 his was a randomized, double-blind, 12-week, crossover study of rosuvastatin 20 mg versus placebo, fo
214 study was nested within a cluster-randomized crossover study of selective digestive decontamination a
215 e randomized into a double-blind four-period crossover study of sustained-release ranolazine 500, 1,0
216                                       A case-crossover study of Swedish cases was conducted to ascert
217 onducted a double-blind, placebo-controlled, crossover study of the effect of the long-acting beta(2)
218 completed a double-blind, placebo-controlled crossover study of the effects of a single dose of amphe
219 al research sites in an open label, 3-period crossover study of three different daily tenofovir regim
220 al dysfunction were enrolled in a randomized crossover study of transfusing autologous, leukoreduced
221 andomized, double-blind, placebo-controlled, crossover study of two weeks of losartan (50 mg q.d.) on
222 double-blind, randomized, placebo-controlled crossover study of UDCA in 17 clinically stable male pat
223 randomized, placebo-controlled, double-blind crossover study on 10 patients with NYHA class II to III
224 randomized, placebo-controlled, double-blind crossover study on 11 patients with New York Heart Assoc
225 zed, double blind, placebo-controlled, 2-way crossover study on 20 subjects with asthma comparing the
226 tain an intervention group of interest, were crossover studies, or were only published in abstract fo
227 d, double-blind, placebo-controlled, partial-crossover study, participants aged 18 to 65 years with a
228                 In this investigator-masked, crossover study, patients with unmet target intraocular
229 , SETTING, AND PARTICIPANTS: A single-blind, crossover study, performed in a hypobaric chamber, to as
230                                              Crossover study sample size calculations using these rat
231                         In this double blind crossover study, shifts in circulating levels of n-3 and
232                                     The case-crossover study showed a statistically significant inver
233             A recent randomized, controlled, crossover study showed that effective treatment of OSA w
234                         In this double-blind crossover study, subanorectic doses of each peptide alon
235                               In the chronic crossover study, subjects with coronary heart disease co
236                     Study 2 was a randomized crossover study that compared 4 diets in 30 volunteers w
237 c-dose study was a randomised, double-blind, crossover study that enrolled adults (aged >/=18 years)
238                In a randomized, double-blind crossover study, the cysteinyl leukotriene antagonist mo
239           In conclusion, in this randomized, crossover study, there was no significant difference in
240          We conducted two placebo-controlled crossover studies to assess the bronchodilator response
241 cohort study and 2 interventional randomized crossover studies to assess: 1) the relationship between
242 lthy volunteers were exposed in a randomized crossover study to 0.3 ppm ozone and clean air for 2 hr
243 lled in a double-blinded, placebo-controlled crossover study to assess the effect of 1200 mg of gamma
244 were enrolled in a bicentric intraindividual crossover study to compare lesion enhancement with doses
245 lind placebo-controlled randomized three-way crossover study to compare the hemodynamic effects of 7
246                          We conducted a case-crossover study to compare the rates of antipsychotic us
247 blind, randomized, placebo-controlled, 2-way crossover study to determine the reversal effect of desc
248                          We conducted a case-crossover study to evaluate the relationship between air
249                          We conducted a case-crossover study to examine the associations of a set of
250 ouble-blind, randomized, placebo-controlled, crossover study to follow spirometry, quality of life qu
251 -period, double-blind, balanced Latin square crossover study to receive placebo, and ranolazine 500,
252            In this randomized, double-blind, crossover study, twelve normoglycaemic men (BMI 25-35 kg
253                        We performed a cohort-crossover study using data on all emergency department v
254 andomized, double-blind, placebo-controlled, crossover study using functional magnetic resonance imag
255                                       A case-crossover study utilizing time-stratified controls was c
256                      A randomized controlled crossover study was conducted in 12 patients with modera
257                  A single-blind, randomized, crossover study was conducted in 30 men and 30 women (30
258 d, double-blind, placebo-controlled, two-way crossover study was conducted in 35 male subjects allerg
259                                       A case-crossover study was conducted in 36 US cities to evaluat
260 andomized, double-blind, placebo-controlled, crossover study was conducted in 80 patients with CAD, c
261 le-blind, placebo-controlled, within-subject crossover study was conducted in healthy adults (n=17).
262 , double-blind, placebo-controlled, 2-period crossover study was conducted with the Vienna Challenge
263                                       A case-crossover study was conducted.
264 andomized, double-blind, placebo-controlled, crossover study was designed to determine the safety and
265          This double blind, Sham-controlled, crossover study was designed to test the hypothesis that
266        A double-blinded, placebo-controlled, crossover study was employed to determine the renal resp
267 ameters in a single-blind placebo-controlled crossover study was investigated.
268                              Subsequently, a crossover study was performed by randomly assigning anot
269                    A randomized, controlled, crossover study was performed in 15 healthy volunteers w
270 d, double-blind, placebo-controlled, two-way crossover study was performed in 22 steroid-naive mild-t
271                     A 3-arm, 12-d randomized crossover study was performed in 30 men and 28 women [me
272                            A 12-d randomized crossover study was performed in 40 men and 39 women [me
273                                            A crossover study was then done in which levodopa-treated
274 se of this double-blind, placebo-controlled, crossover study was to determine age-related differences
275                  The aim of this randomized, crossover study was to determine if transoral fundoplica
276 rpose of this sham-controlled, double-blind, crossover study was to identify the neural circuitry tha
277                                 A randomized crossover study was undertaken with 47 overweight and ob
278                             In a randomized, crossover study, we assigned 13 patients with type 2 dia
279                                         In a crossover study, we assigned 28 participants to outdoor
280                             In a prospective crossover study, we enrolled 33 patients with ischemic c
281              In this randomised, open-label, crossover study, we enrolled preadolescent children (age
282                                 In this case-crossover study, we included the 1316 patients who recei
283                  In a double-blind, 3-period crossover study, we randomly assigned 28 healthy postmen
284              In this open-label, randomised, crossover study, we recruited adults (aged >/=18 years)
285                          In this randomised, crossover study, we recruited men and women aged 60 year
286  Here, in a 6-month double-blind alternating crossover study, we show that bilateral deep brain elect
287                                          Two crossover studies were conducted: 36 participants with t
288                                              Crossover studies were performed 7 to 10 days apart.
289 andomized, placebo-controlled, double-blind, crossover studies were performed for 1 month on patients
290                      Two double-blind, 4-way crossover studies were performed, each of which included
291 es unbiased health-effects estimates in case-crossover studies with shared exposures.
292                         In two random-order, crossover studies with similar but distinct designs, we
293                                         In a crossover study with 7 healthy volunteers, 2 experiments
294       We designed an open-label, randomized, crossover study with blind end point evaluation to compa
295  In this prospective, randomized, open-label crossover study with masked outcome assessments, stable
296  performed a randomized, placebo-controlled, crossover study with prednisolone (40 mg daily) or place
297 randomized, double-blind, placebo-controlled crossover study with single-dose intranasal oxytocin (24
298  healthy men were studied in a single-blind, crossover study with two randomized visits (one with 40
299 ere studied in a randomized, double-blinded, crossover study, with 2-h intravenous administration of
300  Furthermore, in a double-blind, randomized, crossover study, xylitol sprayed for 4 days into each no

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