Actively Recruiting

Age: 18Years - 42Years
FEMALE
NCT04481321

Clinical and Molecular Study of Endometriosis and Adenomyosis

Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-11-20

5300

Participants Needed

1

Research Sites

1804 weeks

Total Duration

On this page

Sponsors

A

Assistance Publique - Hôpitaux de Paris

Lead Sponsor

U

URC-CIC Paris Descartes Necker Cochin

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Clinical and Molecular Study of Endometriosis and Adenomyosis

Who Can Participate

Age: 18Years - 42Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women aged between 18 and 42 years old
  • Receiving care for pelvic pain, infertility, or a pelvic mass
  • Have a radiological diagnosis made by a referral practitioner or have had surgery in the department
Not Eligible

You will not qualify if you...

  • HIV-positive or infected with HBV or HCV
  • Currently pregnant
  • Have a cancer diagnosis
  • Refuse to sign consent

AI-Screening

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Trial Site Locations

Total: 1 location

1

Port Royal, hospital cochin

Paris, France, 75014

Actively Recruiting

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Research Team

C

Charles Chapron, MD

CONTACT

L

Laurence Lecomte, PhD

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

1

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