NCT06553989Recruiting
Impact on Quality of Life of Osteopathic Visceral Mobilizations After Endometriosis Surgery
Impact on Quality of Life of Osteopathic Visceral Mobilizations in Patients Undergoing Post-operative ENDOmetriosis Surgery
Source: ClinicalTrials.gov · Last updated 4 Feb 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 63 (estimated)
- First submitted
- 8 Aug 2024
- Start date
- 27 Jan 2025
- Primary completion date
- Sept 2027
- Lead sponsor
- University Hospital, Clermont-Ferrand
- Diseases
- Endometriosis
- NCT number
- NCT06553989
What you commit to
- Study type: Interventional
- Planned participants: 63
- From 27 Jan 2025 to the primary completion date, Sept 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Indication for surgery for superficial endometriosis
Age
- Patient of legal age, under guardianship or trusteeship
Other
- 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.
Who the study is looking for
- 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)
Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| CHU de Clermont-Ferrand Coordinator of this site? Confirm its status | Clermont-Ferrand | France | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.