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临床试验/ACTRN12615000765527
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

发起方
Professor Roger Hart

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