临床试验/NCT02129894

NCT02129894

Unknown

3 期

The Use of Abdominal Binders in Patients Undergoing Cesarean Sections: A Randomized Controlled Trial

St. Luke's Hospital, Pennsylvania1 个研究点分布在 1 个国家目标入组 210 人2013年11月

适应症Cesarean Section Post Operative Management

概览

阶段: 3 期
干预措施: 未指定
疾病 / 适应症: Cesarean Section Post Operative Management
发起方: St. Luke's Hospital, Pennsylvania
入组人数: 210
试验地点: 1
主要终点: Pain measurement
最后更新: 12年前

概览研究者入排标准结局指标研究点相似试验

概览

简要总结

To see if the use of Abdominal Binders improves patients out comes after cesarean delivery

详细描述

Inclusion: All patients admitted to labor and delivery Consented patients who had a cesarean delivery will be randomized using a number table to receive or not receive an abdominal binder. Outcomes: On postoperative days 1 and 2, patients were asked to complete a pain visual analog scale and the validated Symptom Distress Scale. Postoperative hemoglobin and hematocrit were also recorded.

注册库

clinicaltrials.gov

开始日期

2013年11月

结束日期

2014年10月

最后更新

12年前

研究类型

Interventional

研究设计

Single Group

性别

Female

研究者

发起方

St. Luke's Hospital, Pennsylvania

责任方

Sponsor

入排标准

入选标准

•Women undergoing cesarean section for any indication

排除标准

•unable to give consent

结局指标

主要结局

Pain measurement

时间窗: up to post operateive day 2

Pain will be measured using a visual analog scale

Patient Distress score

时间窗: up to post operateive day 2

A validated patient distress score will be used

次要结局

hemoglobin and hematocrit(post operative day 1 and 2)
Pain medication usage(post operative day 1 and 2)

研究点 (1)

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