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。
研究者
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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