NCT00986089撤回不适用
Pilot Study of Copper IUD Placement at the Time of Cesarean Section
适应症
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 主要终点
- Continuation at one year
研究概览
简要总结
To evaluate the continuation of the Copper IUD at one year after placement through the cesarean incision into the uterus at the time of cesarean section.
研究设计
- 研究类型
- Observational
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 40 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Desire an IUD post-partum and are willing to use the copper IUD.
- •They will also need to be patients at one of our OBGYN clinics at the university of Kentucky.
排除标准
- •Post-partum hemorrhage,
- •Chorioamnionitis (or a fever >101 at the time of cesarean),
- •Women on antibiotic or immunosuppressive therapies,
- •Cervical dilation > 5 cm at the time of c-section, OR
- •Excessive intraoperative blood loss.
- •Also women with contraindications to a copper IUD: Wilson's disease, unusual uterine shape or known uterine anomaly.
结局指标
主要结局
Continuation at one year
时间窗: 1 year
次要结局
- satisfaction with placement at time of cesarean(4-6 months and 1 year)
- bleeding profile(6 months)
研究者
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