Exposure to Persistent Organic Pollutants and Severity of Endometriosis in the ComPaRe-Endometriosis Cohort
NCT ID: NCT06973603
Last Updated: 2025-09-03
Study Results
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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NOT_YET_RECRUITING
650 participants
OBSERVATIONAL
2025-12-31
2026-09-30
Brief Summary
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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.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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Blood samples
24mL blood sample (3 dry tubes with 8mL)
Eligibility Criteria
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Inclusion Criteria
* 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
* 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.
18 Years
ALL
Yes
Sponsors
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Institut National de la Santé Et de la Recherche Médicale, France
OTHER_GOV
Responsible Party
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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
Countries
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Central Contacts
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Facility Contacts
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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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