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
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
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.
研究者
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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