NL-OMON42537已完成3 期
A multi-center, Randomized, double-blind, placebo-controlled study to Evaluate the Safety and efficacy of a single oral dose of vanoxerine for The conversion Of subjects with REcent onset atrial fibrillation or flutter to normal Sinus Rhythm - RESTORE SR
aguna Pharmaceuticals, Inc0 个研究点目标入组 16 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 16
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •Onset of Atrial fibrillation/Atrial Flutter within the 7 calendar days preceding randomisation, based on symptoms. AF/AFL documented by ECG during the screening period and immediately prior to study drug administration. (see protocol page 30)
排除标准
- •See protocol page 30 and 31
研究者
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