ISRCTN35625202已完成1 期
Adverse events, acceptability and efficacy of a combined regimen of ulipristal acetate and misoprostol for abortion through 63 days of gestation
Gynuity Health Projects0 个研究点目标入组 166 人开始时间: 2022年8月16日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 166
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- Female
入选标准
- •1. Pregnant with estimated gestational age =63 days by ultrasound and desiring an abortion
- •2. Body mass index (BMI) =32 kg/m²
- •3. Aged =18 years old or emancipated minor
- •4. With access to a telephone for follow-up communication
- •5. Resident of Mexico City
- •6. Able to provide informed consent
排除标准
- •1. History of hepatic or renal disease
- •2. Confirmation or suspicion of ectopic pregnancy, gestational trophoblastic disease or undiagnosed adnexal mass
- •3. IUD in place
- •4. History of allergy to ulipristal or misoprostol (or other prostaglandins)
- •5. Unwilling to or with significant difficulty preventing return to clinic for follow up
- •6. Unable to provide informed consent
研究者
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