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临床试验/CTRI/2025/12/098750
CTRI/2025/12/098750尚未招募1 期

Evaluating The Efficacy And Safety Of Hysteroscopic Procedures Without Cervical Priming Compared To Misoprostol Cervical Priming In Premenopausal Women: An Equivalent Randomized Controlled Trial

self1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2026年1月1日最近更新:

试验速览

阶段
1 期
状态
尚未招募
发起方
入组人数
80
试验地点
1

研究概览

简要总结

Though Misoprostol has been routinely used prior to hysteroscopy, there are several studies that have concluded that cervical priming is not necessary. There are quite a few Indian studies that have evaluated ease of hysteroscopy after cervical priming with misoprostol. But there aren’t many that have evaluated unprimed cervix. With advancements in design and technology of hysteroscopy, the use of misoprostol can be omitted, as backed up by foreign authors. This study will be performed in Indian setup and help in providing evidence based hysteroscopy.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 50.00 Year(s)(—)
性别
Female

入选标准

  • premenopausal Indicated for diagnostic or Operative hysteroscopy Willing and able to provide informed consent.

排除标准

  • Allergy to prostaglandins Prior cervical surgery Active pelvic infection Pregnancy Anatomical abnormalities (e.g., cervical stenosis, Müllerian anomalies).

研究者

发起方
self
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr Yogita Satpute

All India Institute of Medical Sciences, Nagpur

研究点 (1)

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