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临床试验/ISRCTN37028168
ISRCTN37028168
已完成
未知

A randomised, single-blind clinical trial to investigate the effectiveness of bipolar versus monopolar diathermy treatment on pain symptoms for women with newly diagnosed superficial endometriosis: the SET study (Superficial Endometriosis Treatment)

Portsmouth Hospitals NHS Trust (UK)0 个研究点目标入组 32 人2014年5月7日

概览

阶段
未知
干预措施
未指定
疾病 / 适应症
Gynaecology - Endometriosis
发起方
Portsmouth Hospitals NHS Trust (UK)
入组人数
32
状态
已完成
最后更新
5年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2014年5月7日
结束日期
2015年8月1日
最后更新
5年前
研究类型
Interventional
性别
Female

研究者

发起方
Portsmouth Hospitals NHS Trust (UK)

入排标准

入选标准

  • Preoperative
  • The patient must meet ALL of the following criteria to be considered eligible for the study:
  • 2\. Aged 18 years and above.
  • 3\. Scheduled for diagnostic laparoscopy due to history of pelvic pain (clinical suspicion of endometriosis)
  • 4\. Willing and able to give informed consent for participation in the study
  • Intraoperative
  • The participant must meet ALL of the following criteria to be considered eligible for the study:
  • Superficial endometriosis found at laparoscopy, defined by Stage I or II of the revised American Fertility Society rAFS score.

排除标准

  • Preoperative
  • The patient may not enter the study if ANY of the following apply:
  • 1\. Previous diagnosis of endometriosis from previous surgery/assessment
  • 2\. If language or competency barriers exist during consenting
  • Intraoperative
  • The participant may not enter the study if ANY of the following apply:
  • 1\. Position of endometriosis contraindicates use of either diathermy treatment due to risk of complications, e.g. endometriosis vesicle over the ureter

结局指标

主要结局

未指定

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