Actively Recruiting
Impact on Quality of Life of Osteopathic Visceral Mobilizations After Endometriosis Surgery
Led by University Hospital, Clermont-Ferrand · Updated on 2025-02-04
63
Participants Needed
1
Research Sites
187 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
One of the most common post-operative complications of gynaecological surgery, and in particular endometriosis surgery, is the formation of peritoneal adhesions. After laparotomy, it affects up to 90% of patients. Minimally invasive techniques (such as laparoscopy) reduce the risk of adhesion formation, but cannot totally prevent it. Adhesions can lead to chronic pelvic pain, dyspareunia, digestive disorders and infertility. Various strategies and devices have been developed to try and limit adhesion formation, but their effectiveness has not been fully proven in the literature. The only real treatment for adhesions is adhesiolysis, although adhesions often reform. The quality of surgery remains the best means of preventing adhesion formation. To reduce the morbidity associated with pelvic adhesions, it is essential to develop alternative, non-invasive, anti-adhesive methods such as manual osteopathic visceral mobilization.
CONDITIONS
Official Title
Impact on Quality of Life of Osteopathic Visceral Mobilizations After Endometriosis Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Woman of legal age
- Indication for surgery for infiltrating endometriosis
- Able to give informed consent to participate in research
- Patient included in NO ENDO (national endometriosis observatory promoted by Clermont-Ferrand University Hospital)
You will not qualify if you...
- Indication for surgery for superficial endometriosis
- Patient of legal age, under guardianship or trusteeship
- Pregnant or breast-feeding patient
- Patients not affiliated to the social security system
- Patients who do not speak French
- Patients under court protection
- Simultaneous participation in another study
- Refusal to participate.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
CHU de Clermont-Ferrand
Clermont-Ferrand, France
Actively Recruiting
Research Team
L
Lise Laclautre
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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