CTRI/2020/08/027122尚未招募3 期
Comparison of efficacy of vaginal misoprostol 100 micrograms versus 200 micrograms for cervical priming prior to operative hysteroscopy â?? a randomized control trial.
Internal Fluid Research0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
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
入选标准
- •Patients requiring operative hysteroscopy for intrauterine cavitory pathologies based on transvaginal ultrasound.
排除标准
- •1. Contraindications to hysteroscopy (i.e. pregnancy, cervical malignancy, recent or recurrent pelvic inflammatory disease, marked cervical stenosis, profuse uterine bleeding or recent uterine perforation etc.)
- •2. Any possible contraindications to use of prostaglandins (known sensitivity to prostaglandins, cardiovascular disease, renal failure, severe bronchial asthma, glaucoma etc.)
- •3. Previous cervical surgery
- •4. Presence of significant uterovaginal prolapse impairing vaginal administration.
- •5. Unmarried women where administration of vaginal misoprostol cannot be done.
研究者
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