Franco-European Institute of Endometriosis long-term outcomes cohort

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a prospective, observational, single-center cohort conducted at the Endometriosis Center of Clinique Tivoli-Ducos in Bordeaux, France. Women with histologically or radiologically confirmed pelvic or deep endometriosis are enrolled after consent and complete standardized questionnaires at baseline and at 1, 3, 5, 7, and 10 years, with data collected via the secure NO ENDO online platform or in clinic. The study records treatment choices (medical and surgical), symptom scores, quality-of-life measures, recurrence, and fertility outcomes without altering patient care. The goal is to provide long-term outcome data that are currently scarce in endometriosis research.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* 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

Exclusion Criteria:

* Refusal to participate
* Patients under guardianship or curatorship, or deprived of liberty

Where it's running

• Clinique Tivoli Ducos
  Bordeaux, France Recruiting

Study contacts

• Study coordinator: Horace ROMAN
• Email: horace.roman@ifemendo.fr
• Phone: 0556116000

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.