临床试验/NCT02382952

NCT02382952撤回不适用

Pilot Study Differential Dissector™ for Blunt Dissection

University of North Carolina, Chapel Hill0 个研究点开始时间: 2015年3月最近更新: 2016年8月5日

适应症

试验速览

阶段: 不适用
状态: 撤回
发起方: University of North Carolina, Chapel Hill
主要终点: Post-operative Blood Loss

研究概览研究设计入排标准结局指标研究者记录与标识符相似试验

研究概览

简要总结

The primary purpose of this study is to evaluate the quality of blunt dissection during abdominal and pelvic surgery involving dissection of adhesions, separation of blood vessels and neurovascular structures while preserving the integrity of these structures.

研究设计

研究类型: Interventional
分配方式: Randomized
干预模型: Parallel
盲法: None

入排标准

年龄范围: 18 Years 至 —（Adult, Older Adult）
性别: All
接受健康志愿者: 否

入选标准

•Age greater than 18
•Patient will be undergoing open abdominal surgery
•Patient willing and able to provide his/her own consent

排除标准

•Current alcohol or other substance abuse
•Current incarceration

结局指标

主要结局

Post-operative Blood Loss

时间窗: After surgical closure and drain insertion through drain removal

Operative Blood Loss

时间窗: From start of surgery to wound closure

次要结局

未报告次要终点

研究者

发起方

University of North Carolina, Chapel Hill

申办方类型

Other

责任方

Sponsor

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