ISRCTN44341343已完成不适用
A comparison of vaginal misoprostol versus vaginal misoprostol and nitric oxide donor for termination of pregnancy at 13 to 29 weeks. A prospective randomised trial
Farhat Hached University Teaching Hospital (Tunisia)0 个研究点目标入组 70 人开始时间: 2002年12月16日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 70
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. All patients requiring a termination of pregnancy between 13 and 29 weeks of gestation
- •2. No pregnancy induced hypertension
- •3. No pre-eclampsia
- •4. No vaginal bleeding
- •5. Cervix dilated less then 2 cm
- •6. No vaginal bleeding
- •7. At admission blood pressure: systolic >120 mmHg; diastolic >80 mmHg
排除标准
- •Does not match inclusion criteria
研究者
相似试验
已完成
3 期
A comparison of vaginal misoprostol and vaginal evening primrose oilSpontaneous abortion.Genital tract and pelvic infection following incomplete spontaneous abortionO03.0IRCT20201218049749N1Kashan University of Medical Sciences72
尚未招募
不适用
Comparison of the effect of vaginal misoprostol and evening primrose oil capsules with misoprostol alone on the consequences of abortion in women with intrauterine fetal deaththe consequences of abortion in women with intrauterine fetal death.Medical abortion : complete or unspecified, without complicationO04.9IRCT20181207041873N3Iran University of Medical Sciences84
已完成
不适用
Comparison of 2 different methods in Second trimester labor inductiopregnancy.Pregnancy with abortive outcomeO00-O08IRCT201307159568N5Hormozgan University of Medical Sciences100
已完成
2 期
Comparison the effect of vaginal Misoprostol and vaginal Isoniazid for cervical ripening prior to hysteroscopy proceduresAbnormal uterine and vaginal bleeding, unspecified.Abnormal uterine and vaginal bleeding, unspecifiedIRCT2015112821506N4Iran University of Medical Sciences100
已完成
3 期
Comparison of vaginal estradiol in cervical ripening with misoprostolIRCT20211013052756N1Iran University of Medical Sciences102