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1 's Health Insurance Program (CHIP) coverage (intent-to-treat analyses).
2 s maintenance fluids for 48 hours or longer (intent-to-treat analyses).
3 an immunodeficiency virus (HIV) infection in intent-to-treat analyses.
4 Data were analyzed by intent-to-treat analyses.
5 cts were randomized, with 24 included in the intent-to-treat analyses.
6 ttreatment assessments, and were included in intent-to-treat analyses.
7 and secondary outcomes between groups using intent-to-treat analyses.
8 This effect was not observed in the intent-to-treat analyses.
9 apists were included in the primary modified intent-to-treat analyses.
10 111 placebo) in VISUAL-2 were studied using intent-to-treat analyses.
11 ere randomized to IPT or EUC and included in intent-to-treat analyses.
12 Data were analyzed using intent-to-treat analyses.
13 nts were randomly assigned and considered in intent-to-treat analyses (103 patients in arm A and 101
18 er they attended any treatment sessions (ie, intent-to-treat analyses), and no covariates still showe
19 trial's rationale, study design, and initial intent-to-treat analyses, as well as an explanation of w
21 he post hoc results obtained from stratified intent-to-treat analyses based on maternal vitamin D bas
22 ciated with lower MSI scores at follow-up in intent-to-treat analyses compared with WLC plus treatmen
32 -cause death compared with semaglutide under intent-to-treat analyses (HR, 0.83; 95% CI, 0.69-0.99),
40 ceived the intervention and were included in intent-to-treat analyses; of these, 39 (80%) were female
65 ence generation, allocation concealment, and intent-to-treat analyses were present even in the high-i