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1 Participants were randomly assigned 1:1 by a computer-generat
2 Participants were randomly assigned (
1:1) by a secure website
3 Participants were randomly assigned (
1:1) centrally by an int
4 Participants were randomly assigned (
1:1) in blocks of two us
5 Participants were randomly assigned (
1:1) to active product (
6 Participants were randomly assigned (
1:1) to receive a single
7 Participants were randomly assigned (
1:1) to receive a single
8 Participants were randomly assigned (
1:1) to standard ART ini
9 Participants were randomly assigned (
1:1) within 10 days afte
10 After a 2-4 week run-in period,
participants were randomly assigned (
1:1), using web-based ra
11 Participants were randomly assigned (
1:1), via a computer-gen
12 Participants were randomly assigned (
1:1), via computer-gener
13 Participants were randomly assigned (
1:1:1) to receive a sing
14 Eligible
participants were randomly assigned (
1:1:1) to receive either
15 Participants were randomly assigned (
2:1) by a computer-gener
16 Participants were randomly assigned (
2:1) to intervention or
17 Participants were randomly assigned (
2:1; stratified by sex)
18 Between Aug 8, 2013, and Sept 1, 2015, 161
participants were randomly assigned (
84 to BeatIt; 77 to Step
19 Participants were randomly assigned in a 1:1:1 ratio to once-
20 Participants were randomly assigned to 1 of 4 conditions: clo
21 Participants were randomly assigned to 2 groups: 1 using only
22 2-month phase-in period with repeated baseline assessment,
participants were randomly assigned to 3 months of CBT-I or T
23 Sixty-two male
participants were randomly assigned to a stress condition (Tr
24 Before the futility analysis, 90
participants were randomly assigned to active (n=60) or sham
25 After a 2-wk run-in period,
participants were randomly assigned to consume 1 of 2 weight-
26 Participants were randomly assigned to daily subcutaneous ana
27 Participants were randomly assigned to doxycycline (200 mg pe
28 33
participants were randomly assigned to each group.
29 Between June 23, 2008, and Sept 28, 2012, 125 eligible
participants were randomly assigned to either sodium thiosulf
30 Eligible
participants were randomly assigned to either the artemether
31 Participants were randomly assigned to either the intermitten
32 Participants were randomly assigned to groups given either ol
33 Participants were randomly assigned to groups placed on diets
34 Participants were randomly assigned to iCST (75, 30-min sessi
35 Participants were randomly assigned to one of three groups wh
36 Participants were randomly assigned to receive 1 of 3 (1) sup
37 Participants were randomly assigned to receive a ritonavir-bo
38 Participants were randomly assigned to receive amlodipine, li
39 Participants were randomly assigned to receive either an init
40 6 unmedicated depressed participants and 43 healthy control
participants were randomly assigned to receive either placebo
41 Methods
Participants were randomly assigned to receive high-dose MTX
42 Participants were randomly assigned to receive oral cephalexi
43 1267 eligible
participants were randomly assigned to the brief intervention
44 Between April 14, 2015, and May 5, 2016, 37
participants were randomly assigned to the CGM plus CSII grou
45 ts were randomly assigned to the CGM plus CSII group and 38
participants were randomly assigned to the CGM plus MDI group
46 Participants were randomly assigned to the intervention (TIP)
47 R-E group (mean age, 48.3 years; 72.7% male); a total of 44
participants were randomly assigned to the NR-E group, with 4
48 A total of 44
participants were randomly assigned to the R-E group (mean ag
49 Participants were randomly assigned to treatment for 16 weeks
50 Participants were randomly assigned within BMI categories to
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