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Clinical Trials in France / NCT07179419
Recruiting Observational

Evaluation of the Long-term Therapeutic Effect of High-Intensity Focused Ultrasound (HIFU) Treatment in Patients With Rectal Endometriosis

NCT07179419 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2021-10-10
Last updated
2025-09-17

Condition(s) studied

Endometriosis

Study summary

Evaluate the long-term effects of HIFU treatment for rectal endometriosis.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients who have been treated with HIFU for rectal endometriosis included in study HIFU/F/13.12, study HIFU/F/20.01 (ENDO HIFU R1) or study HIFU/F/21.12 (ENDO HIFU R2) * Agreeing to participate in the study * Patients with internet access so that they can complete the questionnaires electronically. Exclusion Criteria: * Patients deprived of their liberty following a judicial or administrative decision, * Patients under guardianship or conservatorship.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Hopital de la Croix Rousse Lyon France Recruiting

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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 NCT07179419 on ClinicalTrials.gov ↗ ← All trials in France