IRCT201012155401N1已完成2 期
Comparison of Preterm Labor Rate in using Proloton and Vaginal Suppository Progestrone in High Risk Pregnancies
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 100
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
- 年龄范围
- 18 years 至 42 years（—）
- 性别
- Female
入选标准
- •all high risk women for pre-term labour including: recurrent abortion, pre tem labour history, cervical rippening, etc. Exclusion criteria: Epileptic and asthmatic subjects; those with uncontrolled diabetes; those who were sensitive to progesterone; those who have received progesterone four weeks before the study; mental illness; chronic HTN; active liver disorder; HIV infection or 35> CD4 count and anti-viral drug recipients; placenta previa; history of genital and breast cancer; history of thromboembolic disease and mullerian anomaly; ultrasound diagnosed major anomaly; recognized fetal chromosomal abnormalities; Multiple cerclage and preterm labor and PROM and clinical chorioamnionitis; vaginal bleeding and history of spontaneous preterm labor without delivery (including preterm labor).
排除标准
- 未提供
研究者
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