Actively Recruiting
Cohort of the Franco-European Multidisciplinary Institute of Endometriosis
Led by Clinique Tivoli Ducos · Updated on 2025-11-24
15000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Endometriosis is a chronic, non-cancerous gynecological condition that affects 5 to 10% of women of reproductive age and is often linked to pelvic pain, digestive issues, and infertility. This research aims to evaluate the long-term effects of various medical and surgical treatments for deep pelvic endometriosis on symptoms, quality of life, recurrence, and fertility outcomes. It is a prospective, observational, single-center study conducted at the Endometriosis Center of Clinique Tivoli-Ducos in Bordeaux, France. Participants include women with confirmed pelvic endometriosis diagnosed histologically or by imaging. Data is collected through standardized questionnaires completed at the start of the study and then again at 1, 3, 5, 7, and 10 years. The questionnaires cover symptoms, fertility status, and quality of life. Surgical details and complications are also recorded when surgery occurs. Data can be submitted via a secure online platform or paper forms. During the study, participants will complete follow-up questionnaires over a 10-year period. Researchers will monitor symptom changes, digestive function, fertility outcomes, disease progression, and treatment effectiveness. A quality assurance plan ensures data accuracy and completeness. The study aims to improve understanding of endometriosis' natural history and long-term treatment results to enhance patient care.
CONDITIONS
Brief Title
Cohort of the Franco-European Multidisciplinary Institute of Endometriosis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women aged over 18 years
- Women with histologically or radiologically confirmed deep endometriosis and/or infiltrating the colon and/or rectum
- Women affiliated with the social security system
You will not qualify if you...
- Refusal to participate
- Patients under guardianship or curatorship, or deprived of liberty
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 week
Participants undergo confirmation of pelvic endometriosis diagnosis through histological or radiological methods.
1 visit (in-person)
Duration - 10 years
Participants complete questionnaires at inclusion and at 1, 3, 5, 7, and 10 years to evaluate symptoms, quality of life, fertility, and treatment outcomes.
6 questionnaire completions (baseline and 5 follow-up timepoints)
Trial Site Locations
Total: 1 location
1
Clinique Tivoli Ducos
Bordeaux, France, 33000
Actively Recruiting
Research Team
H
Horace ROMAN
C
Clotilde HUET
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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