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Recruiting Not applicable

Identify a Specific Immune Profile in Patients With Chronic Pelvic Pain Resistant to First-line Treatments by Measuring Th1, Th2, Th17, and Treg Cytokines Produced After Non-specific Functional Cell Stimulation - ImmunoCPP

NCT07429773 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2026-04-14
Last updated
2026-07-27

Condition(s) studied

EndometriosisChronic Pelvic Pain Syndrome

Investigational drug(s) / intervention(s)

Immune profile

Immune profile: The immune profile will be determined by measuring blood concentrations (in pg/mL) of pro-inflammatory and anti-inflammatory cytokines measured after non-specific stimulation of peripheral blood cells from each patient: IL4, IL5, IL12p70, 1L17A, IFNγ, IL1β, IL6, IL8, IL10, IL15, IL18, TNFα, TGFβ.

Study summary

Chronic pelvic pain (CPP) affects more than one in four women. An immune imbalance in the Th1/Th2 balance has been reported in multiple CPP situations, particularly in patients with endometriosis, but with mixed results. The use of a functional immune test, already validated in previous indications and particularly in infertility, could simulate an immune stimulation similar to that of painful attacks.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
40 Years
Healthy volunteers
No
Inclusion Criteria: 1. Aged between 18 and 40; 2. Under continuous hormone treatment for at least 6 months; 3. Imaging less than 12 months old: either normal or showing endometriosis and/or adenomyosis lesions, excluding any other abnormalities that could explain the PCOS; 4. Affiliation with the French Social Security system; 5. Signature of informed consent. Exclusion Criteria: 1. Pregnant or breastfeeding women; 2. Autoimmune disease; 3. History of cancer within the last 5 years or currently undergoing treatment; 4. Current infectious syndrome; 5. Person under guardianship or conservatorship.

Primary outcome measure(s)

  • Identify a specific immune profile in patients with chronic pelvic pain, with or without endometriosis, who have failed hormone treatment. — 24 months
    Measurement of blood concentrations (in pg/mL) of pro-inflammatory and anti-inflammatory cytokines measured after non-specific stimulation of peripheral blood cells from each patient: IL4, IL5, IL12p70, 1L17A, IFNγ, IL1β, IL6, IL8, IL10, IL15, IL18, TNFα, TGFβ.

Trial sites (1)

FacilityCityRegionStatus
CHU Nice - Hôpital de l'Archet 2 Nice Alpes-Maritimes Recruiting
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 NCT07429773 on ClinicalTrials.gov ↗ ← All trials in France