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

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

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06973603
Acronym
POPENDO
Enrollment
650
Registered
2025-05-15
Start date
2026-12-01
Completion date
2026-12-01
Last updated
2026-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometriosis

Keywords

exposition, Endometriosis, Organic Persistent Polluant, Endometriosis severity, endomestriosis symptoms, endometriosis pain

Brief 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.

Interventions

OTHERBlood samples

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

Sponsors

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

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Assessment of the severity of endometriosis, defined by the type of disease.During 3 last years of analysisAnalysis 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 sampleChemical 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 sampleChemical 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 sampleChemical 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 sampleChemical analysis of participants' blood samples by the LABERCA laboratory

Secondary

MeasureTime frameDescription
definition of the level of severity of endometriosis by the rASRM stage (revised stage of the American Society for Reproductive Medicine)During 3 last years of analysisAnalysis of online questionnaires on endometriosis and rASRM stage
definition of the level of severity of endometriosis by the anatomical extension of the disease observed on MRIDuring 3 last years of analysisPelvic MRI images will be reviewed by radiologists from Hôpital Paris Saint Joseph to map endometriosis across 21 anatomical structures within 5 pelvic segments, using the ENZIAN classification to assess lesion location and severity.
endometriosis severity level defined by the severity of painful symptoms.During 3 last years of analysisAnalysis of annual follow-up questionnaire of ComPaRe-Endometriosis study participant assessing the severity of various pain types over the past three months using a numeric rating scale.

Countries

France

Contacts

CONTACTFrédérique Perrotte, Principal investigator
fperrotte@ghpsj.fr01 44 12 38 31
STUDY_DIRECTORMARINA Kvaskoff, Dr

Hôpital Paul Brousse

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 17, 2026