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
782 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Endometriosis is a chronic benign gynecological condition affecting 5 to 10% of women of reproductive age, often responsible for pelvic pain, digestive symptoms, and infertility, leading to a significant reduction in quality of life. Despite its high prevalence, the long-term outcomes of different medical and surgical treatments remain poorly documented. The IFEMENDO study is a prospective, observational, single-center, non-interventional cohort conducted at the Endometriosis Center of Clinique Tivoli-Ducos in Bordeaux, France. The objective is to evaluate the long-term efficacy of various therapeutic strategies-both medical and surgical-in terms of symptom improvement, quality of life, recurrence, and fertility outcomes. Women with histologically or radiologically confirmed pelvic endometriosis are invited to participate. Data are collected through standardized questionnaires at baseline and at 1, 3, 5, 7, and 10 years after inclusion, either via the secure NO ENDO online platform or in paper form. The study will contribute to a better understanding of the natural history of endometriosis and the long-term effectiveness of different treatment approaches, ultimately supporting improvements in clinical management and patient care.
CONDITIONS
Official Title
Cohort of the Franco-European Multidisciplinary Institute of Endometriosis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women aged >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
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Trial Site Locations
Total: 1 location
1
Clinique Tivoli Ducos
Bordeaux, France, 33000
Actively Recruiting
Research Team
H
Horace ROMAN
CONTACT
C
Clotilde HUET
CONTACT
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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