JPRN-UMIN000038998已完成2 期
A multicenter, randomized, parallel-group study to assess the safety and efficacy of adhesion prevention device, BAX 602, in preventing adhesion of heart and great vessels to surroundings after placement of extracorporeal ventricular assist device (VAD) - NCVC-BAX602
ational Cerebral and Cardiovascular Center0 个研究点目标入组 30 人开始时间: 2020年1月6日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 30
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
- 12years-old 至 80years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1) Patient falling under either of the contraindications of the study device 2) Patient that is participating or is scheduled to participate during the course of this study in any clinical study involving an investigational product 3) Patient ineligible for participation in this study in the judgment of the Investigator/Subinvestigator
研究者
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