ACTRN12615000765527
Not yet recruiting
Phase 4
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 sites20 target enrollmentJuly 23, 2015
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Chronic Pain
- Sponsor
- Professor Roger Hart
- Enrollment
- 20
- Status
- Not yet recruiting
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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
Exclusion Criteria
- •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
Outcomes
Primary Outcomes
Not specified
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