Use of a New Diagnostic Tool in the Detection and Characterization of Endometriosis Lesions
Launched by UNIVERSITY HOSPITAL, TOULOUSE · Jun 26, 2025
Trial Information
Current as of July 23, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial is exploring a new way to better detect and understand endometriosis, a condition where tissue similar to the lining inside the uterus grows outside it, often causing pain. The study is testing a special type of imaging scan called \[18F\]-FES PET/CT, which might be more accurate than current methods like MRI. This scan could help doctors see the disease more clearly and measure how certain hormone receptors (estrogen receptors) are involved, which might also relate to how much pain a patient feels. The goal is to improve diagnosis and guide better treatment choices.
Women over 18 who have endometriosis and are scheduled for surgery may be eligible, especially if they have pain related to the condition or are being treated for infertility. Participants need to have had a recent MRI and be able to undergo the new scan safely. The study will exclude those who are pregnant, menopausal, on hormone therapy, or have certain sensitivities or conditions like claustrophobia. If you join, you can expect to have the new imaging scan before your surgery, which will help researchers understand your condition better. This study is not yet recruiting but aims to make diagnosis and treatment of endometriosis easier and more personalized in the future.
Gender
FEMALE
Eligibility criteria
- 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
About University Hospital, Toulouse
The University Hospital of Toulouse is a leading academic medical center dedicated to advancing healthcare through innovative research and clinical trials. With a strong emphasis on patient-centered care, the hospital integrates cutting-edge scientific inquiry with comprehensive clinical services. Its multidisciplinary team of healthcare professionals collaborates with renowned researchers to facilitate pioneering studies across various medical fields, aiming to enhance treatment options and improve patient outcomes. As a prominent institution in the region, the University Hospital of Toulouse is committed to fostering an environment of excellence in both education and research within the healthcare community.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Toulouse, , France
Patients applied
Trial Officials
Ariane WEYL, MD
Principal Investigator
CHU Toulouse
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported