ACTRN12615000765527尚未招募4 期
Prospective double blind randomised controlled trial of the long-term follow-up of pain post laparoscopic surgery for moderate to severe endometriosis, comparison of standard anaesthesia versus pro-active aggressive intra-operative analgesic intervention, with blinding of surgeon and patient – Pilot Study.
Professor Roger Hart0 个研究点目标入组 20 人开始时间: 2015年7月23日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 20
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
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 40 Years(—)
- 性别
- Female
入选标准
- •Women aged 18-40 who complain of regular significant dysmenorrhea and / or pelvic pain that has persisted for more than 1 year AND
- •Who have undergone a staging laparoscopy according to the AFS endometriosis score by a gynaecologist and are documented to have an American Fertility Society Score of 2 or 3. AND
- •Planned surgery for treatment of endometriosis
排除标准
- •Allergy or sensitivity to methadone or bupivacaine OR
- •Contraindication to use of opioids OR
- •Surgical procedure other than laparoscopic treatment of endometriosis, check of tubal patency and minor hysteroscopic procedure OR
- •Active or relapsing pelvic inflammatory disease OR
- •Poor communication of written and spoken English for informed consent purposes
研究者
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