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Taking people in FranceNo phase

Studying endometriosis and adenomyosis over time in women

Follows women with endometriosis or adenomyosis to see how symptoms and lesions change.

Plain-language title generated from the registry record
Registry title: Clinical and Molecular Study of Endometriosis and Adenomyosis

Key facts

Where
Paris, 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 42 years old?

Source: NCT04481321, who can take part

Where in France

  • Port Royal, hospital cochinParis, 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
Assistance Publique - Hôpitaux de Paris
Trial code
NCT04481321
Record updated
20 November 2025
Original description
The purpose of this study is to determine whether endometriosis and adenomyosis are progressive diseases, in terms of symptoms (pain, abnormal uterine bleeding and infertility), anatomical lesions size, and recurrences. We also aimed to address molecular questions on immune dialogues between ectopic lesions and the eutopic endometrium, auto-immunity in endometriosis and adenomyosis and the role of the microbiota in their respective pathophysiologies.Read full original descriptionShow less

ENDOCHAP Monocentric Cohort: Clinical and Molecular Study of Endometriosis and Adenomyosis

The purpose of this study is to determine whether endometriosis and adenomyosis are progressive diseases, in terms of symptoms (pain, abnormal uterine bleeding and infertility), anatomical lesions size, and recurrences. We also aimed to address molecular questions on immune dialogues between ectopic lesions and the eutopic endometrium, auto-immunity in endometriosis and adenomyosis and the role of the microbiota in their respective pathophysiologies.

Inclusion: Women of age between - 18 and 42 years old; In-service care for one of the pelvic pain and/or infertility, or for a pelvic mass; Having a radiological diagnosis made by a referral practitioner and/or operated in the department.

Exclusion: HIV-positive women, HBV and HCV; Having a cancer diagnosis; During pregnancy; Refusing to sign a consent.

ClinicalTrials.gov NCT04481321