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1 lude data of participants lost to follow-up (intention-to-treat analyses).
2 ) and their infants in efficacy analyses, by intention-to-treat analyses.
3 4 (67 per arm) were included in the modified intention-to-treat analyses.
4 assessment and were included in the modified intention-to-treat analyses.
5 ssessments and were included in the modified intention-to-treat analyses.
6 the conservative group were included in the intention-to-treat analyses.
7 were excluded, leaving 1774 patients for the intention-to-treat analyses.
8 and mean arterial pressure after 2 years in intention-to-treat analyses.
9 assigned and vaccinated were included in the intention-to-treat analyses.
10 ns and all participants were included in the intention-to-treat analyses.
11 n may have contributed to neutral results in intention-to-treat analyses.
12 tion models were used to compare outcomes in intention-to-treat analyses.
13 47% (95% confidence interval, 30-65) in the intention-to-treat analyses.
14 re for at least 1 month were included in the intention-to-treat analyses.
15 otherapy group were included in the modified intention-to-treat analyses.
16 -up comparing screening versus usual care in intention-to-treat analyses.
17 ere used to estimate the treatment effect in intention-to-treat analyses.
18 Seventy patients were included in the intention-to-treat analyses.
19 d with texts revised in the control group in intention-to-treat analyses.
20 e Impact Scale (MFIS) at 12 months) based on intention-to-treat analyses.
21 for Dementia (DAD) scale at time-2, based on intention-to-treat analyses.
22 tudy, leaving 123 patients available for the intention-to-treat analyses.
23 We did intention-to-treat analyses.
24 We performed intention-to-treat analyses.
25 Forty-nine participants were included in intention-to-treat analyses.
26 th, death, and CD4% and growth changes using intention-to-treat analyses.
27 and 93 patients to SDS, and were included in intention-to-treat analyses.
28 nresponse to treatment were determined using intention-to-treat analyses.
29 We used intention-to-treat analyses.
30 c randomized effectiveness trial design with intention-to-treat analyses.
31 bo (n=476), all of whom were included in the intention-to-treat analyses.
32 se findings were supported by the results of intention-to-treat analyses.
33 , and Hungary; all patients were included in intention-to-treat analyses.
34 weight change analyzed by both completer and intention-to-treat analyses.
35 sample sizes, blinding, control groups, and intention-to-treat analyses.
36 We did both per-protocol and intention-to-treat analyses.
37 one dose of study drug were included in the intention-to-treat analyses.
38 omization, of whom 2482 were included in the intention-to-treat analyses.
39 2 (HSV-2) at 18 months and were assessed by intention-to-treat analyses.
40 er percentages and logrank p values are from intention-to-treat analyses.
41 o AHCT, whereas the prospective studies were intention-to-treat analyses.
42 ffect of supplement group on child growth in intention-to-treat analyses.
43 three treatment groups in both on-study and intention-to-treat analyses.
46 patients, 100 were included in the modified intention-to-treat analyses (49 in the open surgery grou
58 g the Kaplan-Meier method and Cox models in "intention-to-treat" analyses and in generalized linear m
64 randomized, 401 contributed to the modified intention-to-treat analyses at year 3 (primary outcome),
69 ts were retained and included in the primary intention-to-treat analyses (control, n = 1,845; self-se
70 ity of studies and by lack of the following: intention-to-treat analyses, data on clinical end points
78 diagnosed with HIV <=30 days prior and used intention-to-treat analyses for the outcomes: proportion
79 , 215, and 217 patients were included in the intention-to-treat analyses for TIO monotherapy, UMEC mo
80 , 214, and 212 patients were included in the intention-to-treat analyses for TIO monotherapy, VI mono
83 s were significantly improved from baseline, intention-to-treat analyses found no overall differences
84 ignificantly different between groups in the intention-to-treat analyses (HR: 0.84; 95% CI: 0.58, 1.2
87 ts withdrew prior to treatment, the modified intention-to-treat analyses included 111 participants (9
96 sing random-effects mixed-regression models, intention-to-treat analyses indicated no significant cha
97 ilevel, mixed-effects linear regression with intention-to-treat analyses is presented.SIPsmartER part
99 total of 3365 patients were included in the intention-to-treat analyses (median treatment duration,
110 trast, in April 2001, the company's internal intention-to-treat analyses of pooled data from these 2
111 We report here the per-protocol and modified intention-to-treat analyses of the prespecified secondar
113 nd stratified log-rank methods were used for intention-to-treat analyses of time until the main outco
117 nce weekly, etap2 = 0.068, P = .001) and the intention-to-treat analyses relative to the wait-list co
144 he study, 1089 were included in the modified intention-to-treat analyses (thymosin alpha1 group n=542
189 The results were materially unchanged in intention-to-treat analyses with inverse probability wei