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1 Previously untreated patients with ES SCLC were randomly assigned in a 1:1 fashion to receive carboplati
2 ged Percutaneous Coronary Intervention) trial, 584 patients were randomly assigned in a 1:1 manner to 1S-PCI or MS-PCI.
3 Enrolled patients received surgery for GPi DBS and then were randomly assigned in a 1:1 ratio (computer-generated pai
4 Eligible patients with native papilla undergoing ERCP were randomly assigned in a 1:1 ratio (with a computer-genera
7 on pirfenidone (at least 1602 mg/day for 8 weeks or longer) were randomly assigned in a 1:1 ratio by interactive voice re
9 ipants from Ontario, Canada, experiencing recurrence of CDI were randomly assigned in a 1:1 ratio to 14 days of oral vanc
11 December 2007, enrolled 168 patients with high-risk PCa who were randomly assigned in a 1:1 ratio to conventional (80 Gy
15 s, patients with ST-segment elevation myocardial infarction were randomly assigned in a 1:1 ratio to receive EES or BMS.
19 breast cancer receiving treatment with aromatase inhibitors were randomly assigned in a 1:1 ratio to receive either denos
20 In the phase 2 part of the study, patients were randomly assigned in a 1:1 ratio to receive either olara
22 previously received a regimen containing an NS5A inhibitor were randomly assigned in a 1:1 ratio to receive either the n
23 previously received a DAA regimen but not an NS5A inhibitor were randomly assigned in a 1:1 ratio to receive sofosbuvir-v
24 th an estimated GFR of 25 to 44 ml per minute per 1.73 m(2) were randomly assigned in a 1:1 ratio to receive tolvaptan or
26 0 to 1), stratified by histology (epithelioid or biphasic), were randomly assigned in a 1:1 ratio to up to six cycles of
27 Following 2 weeks of open placebo run-in, patients were randomly assigned in a 1:1 ratio with a block size of 4
28 n, aged 16 years or older and with newly diagnosed epilepsy were randomly assigned in a 1:1 ratio, via a computer-generat
30 icin-sensitive, previously untreated pulmonary tuberculosis were randomly assigned in a 1:1:1:1:2 ratio to receive (all o
35 Patients who were taking a stable dose of methotrexate were randomly assigned in a 2:1 ratio to receive either adali
36 nts with hereditary angioedema with C1 inhibitor deficiency were randomly assigned in a 2:1 ratio to receive either lanad
37 nd non-gBRCA cohort) and the type of non-gBRCA mutation and were randomly assigned in a 2:1 ratio to receive niraparib (3
39 superficial femoral and popliteal peripheral artery disease were randomly assigned in a 2:1 ratio to treatment with DCB o
40 2-4 years in urban Kamalapur and rural Matlab, Bangladesh, were randomly assigned in a 2:1 ratio, according to a compute
42 eatment-naive patients with pulmonary arterial hypertension were randomly assigned in a 2:1:1 ratio and received combinat
45 second-generation healthy women of Mexican descent (n = 53) were randomly assigned in a crossover design to consume a Mex
46 risk patients receiving HPS followed in a tertiary HPS unit were randomly assigned in a double-blinded, placebo-controlle
47 agnetic resonance imaging (MRI)-documented lacunar infarcts were randomly assigned in a factorial design to target levels
49 in the upper third of the albumin-to-creatinine ratios; 443 were randomly assigned in a placebo-controlled trial of an AC
50 In the second cohort, participants with CIC were randomly assigned in a study across four centres with si
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