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This study was designed as a multicenter, randomized, double-blind, placebo-controlled trial.
This study is designed as a multicenter trial, with biological assignment to one of two study arms; Arm 1: Reduced intensity conditioning allogeneic hematopoietic cell transplantation (RIC-alloHCT), Arm 2: Non-Transplant Therapy/Best Supportive Care.
The study was designed as a multicenter, open-label randomised controlled trial to compare the efficacy and safety of gatifloxacin versus azithromycin for the treatment of uncomplicated typhoid fever in children and adult in-patients in southern Vietnam.
The study was designed as a multicenter case control study.
The study is designed as a multicenter prospective observational cohort study.
The study was designed as a multicenter, randomised, open-label phase III trial.
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This study was designed as a prospective multicenter randomized comparison of procedure-related complications, patient recuperation, and quality-of-life outcomes between patients undergoing vein stripping with high ligation and patients undergoing great saphenous vein (GSV) obliteration with temperature-controlled radiofrequency ablation without adjunctive high ligation (Closure procedure).
This study is designed as a nationwide multicenter observational cohort study.
It was designed as a retrospective multicenter study, and clinical manifestations could only be categorized on an all-or-none basis, instead of more a sophisticated standardized scoring system.
The study was designed as a national multicenter cross-sectional study and was conducted between the months of May 2004 and December 2005 among a convenient sample of male and female prison inmates and officers stationed at eight of the ten regional central prisons in Ghana.
This prospective study was designed as a longitudinal multicenter observational cohort study in 42 German hospitals to determine the time to AT, surgical source control and compliance with sepsis recommendations related to AT in patients with suspected severe sepsis or septic shock and its impact on 28-day, ICU, and hospital mortality.
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CEO of Professional Science Editing for Scientists @ prosciediting.com