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Design: A randomized parallel group study.
Study Design and Settings: In a prospective parallel group study, 51 patients with uvulopalatoplasty or tonsillectomy were studied.
The study was designed as a randomized, controlled, parallel group study.
The study was a Phase I trial conducted as randomized, double-blind, placebo-controlled, outpatient, parallel group study.
The study was designed as an open parallel group study.
SERVE-HF is a multinational, multicentre, randomized, parallel group study.
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A double-blind, placebo-controlled, parallel-group study.
The oral RCT with lasmiditan was a randomised, double-blind, placebo-controlled, parallel-group study [17].
Methods: 16-week, multicenter, randomized, double-blind, placebo-controlled, parallel-group study in adults with EM.
The study was designed as a parallel-group study with balanced allocation ratio (1 1).
This is an open-label, two parallel-group study.
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