Actively Recruiting
Is Laparoscopic Excision for Peritoneal Endometriosis Helpful or Harmful?
Led by University of Aarhus · Updated on 2024-11-15
100
Participants Needed
5
Research Sites
230 weeks
Total Duration
On this page
Sponsors
U
University of Aarhus
Lead Sponsor
A
Aarhus University Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
The trial seeks to test effect of laparoscopic excision of peritoneal endometriosis on pelvic pain. Data will also be gathered on quality of life and neuropathic pain. Patients will be randomized to one of three groups: 1) laparoscopy with excision of endometrial tissue, 2) laparoscopy without excision of endometrial tissue and 3) waiting list control.
CONDITIONS
Official Title
Is Laparoscopic Excision for Peritoneal Endometriosis Helpful or Harmful?
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult (≥ 18 years) with suspected peritoneal endometriosis undergoing elective surgery for pain relief
- Pain intensity ≥ 5 on Numeric Rating Scale (NRS) in the four weeks prior to giving consent
You will not qualify if you...
- Other known conditions/diseases that may cause pelvic pain
- Diagnosed personality disorder, schizophrenia or treatment with anti-psychotics
- Planned pregnancy during study period
- Women who cannot read or speak Danish
AI-Screening
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Trial Site Locations
Total: 5 locations
1
Regional Hospital Horsens, Department of Obstetrics and Gynecology
Horsens, Central Jutland, Denmark, DK-8700
Actively Recruiting
2
Aarhus University Hospital, Department of Obstetrics and Gynecology
Aarhus N, Denmark, DK-8200
Actively Recruiting
3
Regional Hospital Herning, Department of Obstetrics and Gynecology
Herning, Denmark, DK-7400
Actively Recruiting
4
Regional Hospital Randers, Department of Obstetrics and Gynecology
Randers, Denmark, DK-8930
Actively Recruiting
5
Regional Hospital Viborg, Department of Obstetrics and Gynecology
Viborg, Denmark, DK-8800
Actively Recruiting
Research Team
H
Henrik Marschall, MSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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