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Starting soon Observational

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

NCT06973603 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2026-12
Last updated
2026-09-16

Condition(s) studied

Endometriosis

Investigational drug(s) / intervention(s)

Blood samples

Blood samples: 24mL blood sample (3 dry tubes with 8mL)

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
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.

Primary outcome measure(s)

  • Assessment of the severity of endometriosis, defined by the type of disease. — During 3 last years of analysis
    Analysis of several online questionnaires on endometriosis by participants
  • Evaluation of serum levels of polychlorinated biphenyls (PCBs) — 5 months after inclusion start until analysis of the last participant' blood sample
    Chemical analysis of participants' blood samples by the LABERCA laboratory
  • Evaluation of serum levels of per- and polyfluoroalkylates (PFAS) — 5 months after inclusion start until analysis of the last participant' blood sample
    Chemical analysis of participants' blood samples by the LABERCA laboratory
  • Evaluation of serum levels of Brominated flame retardants polluent (BFRs) — 5 months after inclusion start until analysis of the last participant' blood sample
    Chemical analysis of participants' blood samples by the LABERCA laboratory
  • Evaluation of serum levels of organochlorine pesticides (POCs) — 5 months after inclusion start until analysis of the last participant' blood sample
    Chemical analysis of participants' blood samples by the LABERCA laboratory

Trial sites (1)

FacilityCityRegionStatus
Hôpital Paris Saint Joseph Paris France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06973603 on ClinicalTrials.gov ↗ ← All trials in France