Under construction – not a live service
Sign in
Taking people in FranceNo phase

Studying Stem Cells and Estrogen in Endometriosis Lesions

Studies cells from the womb lining in women with endometriosis to understand how it starts.

Plain-language title generated from the registry record
Registry title: Endometriosis Transcriptomic Cell Atlas

Key facts

Where
Toulouse, FranceSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 45 years old?

Source: NCT06502548, who can take part

Where in France

  • University Hospital, ToulouseToulouse, FranceTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
University Hospital, Toulouse
Trial code
NCT06502548
Record updated
5 November 2026
Original description
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.Read full original descriptionShow less

Establishing an Endometriosis Transcriptomic Cell Atlas to Decipher the Pathophysiological Role of Stem Cells and Estrogens in the Disease

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.

Inclusion: 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: Patients with endometriosis receiving hormonal treatment at the time of surgery or having received hormonal treatment in the 2 months prior to surgery; Healthy non-endometriotic patients undergoing hysterectomy for infectious or malignant causes; Patients with positive serology for human immunodeficiency virus (HIV), human T-lymphotropic virus (HTLV), hepatitis B (HBV) and hepatitis C (HCV); Patients with endometriosis non-surgically treated; Patients with adenomyosis only; Patients benefiting from a legal protection measure (guardianship, curatorship, safeguard of justice).

ClinicalTrials.gov NCT06502548