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Clinical Trials in France / NCT07053982
Recruiting Not applicable

Use of a New Diagnostic Tool in the Detection and Characterization of Endometriosis Lesions

NCT07053982 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2026-03-23
Last updated
2026-03-25

Condition(s) studied

Endometriosis

Investigational drug(s) / intervention(s)

Preoperative [18F]-FES PET/CT Imaging and Estrogen Receptor Expression Analysis in Endometriosis Surgery

Preoperative [18F]-FES PET/CT Imaging and Estrogen Receptor Expression Analysis in Endometriosis Surgery: This study includes preoperative \[18F\]-FES PET/CT imaging to assess estrogen receptor expression in endometriosis patients undergoing laparoscopic or robot-assisted surgery. Pain levels will be evaluated using VAS, BPI, HADS, and SF-36 scales. Immunohistochemistry and quantitative mRNA expression analysis (ESR1, ESR2, GPER) will be performed on excised lesions using Tissue Microarray. This approach aims to correlate PET/CT imaging findings with histological and molecular data, distinguishing it from standard surgical interventions.

Study summary

Diagnostic wandering is one of the characteristics of endometriosis due to great anatomical and clinical variability but also due to poorly relevant diagnostic examinations. \[18F\]-FES PET/CT could on the one hand improve diagnosis by showing greater sensitivity than MRI and on the other hand make it possible to quantify and characterize the expression of ER from diagnosis and thus helping to guide therapeutic care. We will thus attempt to correlate the intensity of \[18F\]-FES PET/CT with the expression of estrogen receptors and the intensity of pain.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: Cases: \- Painful patients with a VAS ≥ 4 treated surgically for painful symptoms related to endometriosis; Controls: * Patient with a VAS \< 4 treated surgically for endometriosis in the context of infertility; * Age \> 18 years; * Patient who provided informed consent; * Patients who underwent a preoperative MRI and were not contraindicated for \[18F\]-FES PET/CT; * Patient who underwent surgery mid-cycle; * Affiliation to a social security scheme Exclusion Criteria: * Patient treated for endometriosis without surgery; * Pregnant patient * Patient taking hormone therapy * Menopausal patient * Hypersensitivity to the active substance (Fluoroestradiol (18F)) or to any of the excipients * Patient under legal protection * Claustrophobic patient

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Toulouse, Rangueil Hospital Toulouse France Recruiting

More University Hospital, Toulouse trials in France

Other trials for the same condition

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 NCT07053982 on ClinicalTrials.gov ↗ ← All trials in France