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 人开始时间: 2014年5月7日最近更新: 2020年9月14日

适应症

试验速览

暂无简介。

•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.

•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

发起方

Portsmouth Hospitals NHS Trust (UK)