NCT01685593已完成不适用
A Controlled Randomized Trial Examining the Ability of the Mott Compression Bonder to Decrease Postoperative Pain in Gynecologic Abdominal Laparotomy Patients.
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 76
- 试验地点
- 1
- 主要终点
- postoperative pain
研究概览
简要总结
We conducted a controlled randomized trial examining the ability of the Mott abdominal Compression Binder to decrease postoperative pain in gynecologic abdominal laparotomy patients
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Single (Investigator)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •gynecologic abdominal laparotomy patients
排除标准
- •non gynecologic abdominal laparotomy patients
研究组 & 干预措施
regular bandage
Sham Comparator
no abdominal binder
干预措施: no binder (Other)
abdominal binder
Experimental
binder
干预措施: abdominal binder (Device)
结局指标
主要结局
postoperative pain
时间窗: 24 hours
linear pain scale
次要结局
- ambulations in 24 hours postoperatively(24 hours)
研究者
Edward R. Kost, M.D.
Principal Investigator
Brooke Army Medical Center
研究点 (1)
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