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NCT06445179Recruiting

ENDOmetriosis Robotic Assisted Surgery

Robot-Assisted Versus Standard Laparoscopic Approach of Total Hysterectomy for Deep Infiltrating Endometriosis and Adenomyosis: A Multicenter, Open-label Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 20 Jan 2026

Brief summary (registry, in English)

The purpose of this study is to compare the robot-assisted approach with the laparoscopic approach in terms of reducing the rates of intraoperative and postoperative complications in patients undergoing total hysterectomy for DIE and adenomyosis without digestive tract involvement.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
224 (estimated)
First submitted
27 May 2024
Start date
16 Apr 2025
Primary completion date
Jun 2027
Lead sponsor
GCS Ramsay Santé pour l'Enseignement et la Recherche
NCT number
NCT06445179

What you commit to

  • Study type: Interventional
  • Planned participants: 224
  • From 16 Apr 2025 to the primary completion date, Jun 2027
  • 2 sites 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

  • Contraindications to surgery.

Other

  • Digestive tract involvement.
  • Adenomyosis only.
  • Participants who are under guardianship, curatorship, or deprivation of liberty.

Who the study is looking for

  • ≥ 18 years of age.
  • Diagnosed adenomyosis, either internal or external (magnetic resonance imaging) per the Enzian and dPEI classifications.
  • Diagnosed deep infiltrating endometriosis per the Enzian and dPEI classifications, without the involvement of the digestive tract.
  • Failure of first- and second-line medical treatment.
  • Eligibility for total hysterectomy with complete removal of endometriosis lesions.
  • Participants covered by entitled to social security.
  • All participants must provide written informed consent before undergoing the surgical procedure.

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hopital Prive de Provence
Coordinator of this site? Confirm its status
Aix-en-ProvenceFranceRecruiting
Hôpital Privé Le Bois
Coordinator of this site? Confirm its status
LilleFranceRecruiting

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.