NCT01497756已完成不适用
Feasibility Trial of the Circumferential Abdominal Pelvic Pressure Device (CAPP)
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 10
- 试验地点
- 2
- 主要终点
- Usage
研究概览
简要总结
A group of midwives and obstetric nurses have been trained to use circumferential abdominal pelvic pressure (CAPP) to treat postpartum hemorrhage. As part of the training follow up any use of a CAPP device will be monitored to identify complications.
详细描述
Providers will be surveyed twice at 4 and 8 months using open ended methods.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Any patient receiving CAPP during study period.
排除标准
- •None (CAPP is only clinically indicated for obstetric hemorrhage post delivery.
结局指标
主要结局
Usage
时间窗: Eight months
Number of patients on whom CAPP is used
次要结局
- Side Effects(Eight months)
研究者
Mark Hauswald
Professor
University of New Mexico
研究点 (2)
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