ISRCTN61551511进行中（未招募）不适用
A prospective, randomized, controlled trial to evaluate the efficacy, tolerability, and feasibility of a single-use disposable hysteroscopic operating system in an outpatient office setting
Azienda Usl Toscana Centro0 个研究点目标入组 144 人开始时间: 2025年11月15日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 144
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 80 Years（—）
- 性别
- Female
入选标准
- •Female patients scheduled for outpatient diagnostic or operative office hysteroscopy due to suspected intra-uterine pathology (e.g., endometrial polyps, uterine septum, abnormal uterine bleeding [AUB], or thickened endometrium)
- •Age between 18 and 80 years
- •Provided written informed consent prior to study enrollment
排除标准
- •Severe pelvic organ prolapse
- •Active pelvic inflammatory disease (PID) or lower genital tract infection
- •Confirmed or suspected ongoing pregnancy
- •Inability to understand the study protocol or refusal to sign the written informed consent
研究者
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