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Recruiting NCT06502548

Endometriosis Transcriptomic Cell Atlas

Trial Parameters

Condition Endometriosis
Sponsor University Hospital, Toulouse
Study Type INTERVENTIONAL
Phase N/A
Enrollment 92
Sex FEMALE
Min Age 18 Years
Max Age 45 Years
Start Date 2024-09-27
Completion 2027-09
Interventions
EndometriosisTubal ligation or Hysterectomy

Brief Summary

Endometriosis is an estrogen-dependent, chronic inflammatory gynecologic disease affecting women of reproductive age, with a therapeutic wandering of 6 to 10 years. A better understanding of the initiation phase is a major challenge to improve diagnosis and treatment. The most widely accepted hypothesis to explain the formation of endometriotic lesions is the tubal retrograde reflux during menstruation. However, only 10% of the reproductive age women will develop endometriosis while 90% of women experience retrograde menstruation. This raises the question of the stem cells present in the endometrium and menstrual reflux of these patients, but also of both the peritoneal microenvironment and the estrogenic local signaling which allow the implantation of these lesions.

Eligibility Criteria

Inclusion Criteria: * Patients over 18 and under 45 years of age * Patients with multiple endometriosis sites (superficial, deep and endometriomas) with an indication for surgery to treat disabling painful symptoms and stage III or IV endometriosis in the context of infertility. * Healthy patients including those operated on between the ages of 18 and 45 for tubal ligation * Healthy patients operated on between the ages of 18 and 45 for hysterectomies for benign causes other than endometriosis or adenomyosis * Patients operated on strictly at the time of menstruation * Participants who have not been on hormonal treatment for 2 months * Participant having signed the free and informed consent form * Membership of a Social Security scheme or equivalent Exclusion Criteria: * Patients with endometriosis non-surgically treated * Patients with endometriosis receiving hormonal treatment at the time of surgery or having received hormonal treatment in the 2 months prior to surgery * Patients wit

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