Exposure to Persistent Organic Pollutants and Severity of Endometriosis in the ComPaRe-Endometriosis Cohort

NCT ID: NCT06973603

Last Updated: 2025-09-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

650 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-12-31

Study Completion Date

2026-09-30

Brief Summary

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Endometriosis is a chronic inflammatory disease affecting \~10% of women of childbearing age. It is characterized by the presence of endometrial-like tissue outside the uterus, causing lesions and adhesions between the organs, and is often accompanied by intense pain and sometimes infertility. The four-stage classification based on the severity of lesions does not always reflect the severity of symptoms. Adenomyosis, a similar pathology, is often present in the same patients, although it is now considered distinct from endometriosis. Diagnosis usually takes a long time, with an average delay of 7 years. The cause of the disease remains unknown, but hormonal, genetic and environmental factors, such as exposure to endocrine disruptors, are suspected. Persistent organic pollutants (POPs), such as dioxins and PCBs, may influence the risk and severity of the disease. Although experimental studies suggest a link between these substances and the progression of endometriosis, epidemiological research on the subject is still limited.

The central hypothesis of the POPENDO project is that higher concentrations of persistent organic pollutants (POPs) are associated with increased severity of endometriosis. The aim of the study is to explore the associations between serum levels of four families of POPs (PCBs, organochlorine pesticides, PFAS and BFR) and endometriosis.

Detailed Description

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Conditions

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Endometriosis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Blood samples

24mL blood sample (3 dry tubes with 8mL)

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* ComPaRe participants ⩾ 18 years old. All ComPaRe participants are at least 18 years of age, so our research participants will all be adults.
* Having declared in ComPaRe that they had endometriosis
* Living in the Ile-de-France region (departments 75, 77, 78, 91, 92, 93, 94 or 95);
* Have given electronic consent stating: "By checking this box, I agree to be solicited for research outside ComPaRe"; This criterion is collected at the time of ComPaRe registration, when consent is collected. Participants can withdraw this consent at any time on their secure personal online account on the ComPaRe platform.
* Aged ≤ 45 years to avoid including premenopausal or menopausal women;
* In possession of MRI images used to diagnose their endometriosis (CD-ROM) that are no more than 5 years old;
* Enrolled in or benefiting from a social security scheme.

Exclusion Criteria

* \- People with contraindications to blood sampling will not be included in this research:
* Known severe anemia
* Hemophilia/coagulation disorders/anticoagulant use
* People with HIV, HBV or HCV will not be included in this study due to the risk of BSE (Blood Exposure Accident).
* Based on factors that may disrupt lipid dynamics and lipid pollutants, the following individuals will not be included:
* Pregnant and breast-feeding women
* People suffering from any of the following diseases:

* Cancer
* Morbid obesity (BMI\>40)
* Non-alcoholic steatohepatitis (NASH)
* Persons under court protection/guardianship/guardianship will not be able to participate in this research.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Institut National de la Santé Et de la Recherche Médicale, France

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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MARINA Kvaskoff, Dr

Role: STUDY_DIRECTOR

Hôpital Paul Brousse

Locations

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Hôpital Paris Saint Joseph

Paris, , France

Site Status

Countries

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France

Central Contacts

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Frédérique Perrotte, Principal investigator

Role: CONTACT

01 44 12 38 31

Facility Contacts

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Frédérique Perrotte, IP

Role: primary

01 44 12 38 31

Other Identifiers

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ID-RCB

Identifier Type: OTHER

Identifier Source: secondary_id

C24-04

Identifier Type: -

Identifier Source: org_study_id

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