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

E

EDAP TMS

Status

Enrolling

Conditions

Endometriosis

Study type

Observational

Funder types

Industry

Identifiers

NCT07179419
HIFU/F/21.04

Details and patient eligibility

About

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

Full description

This study evaluates the long-term effects of HIFU treatment on endometriosis symptoms in patients who have received this treatment. The patients included will have participated in the following studies: HIFU/F/13.12, ENDO HIFU R1, and ENDO HIFU R2.

Patients will complete an electronic questionnaire and receive a telephone call to monitor these parameters.

Enrollment

140 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial contacts and locations

1

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Central trial contact

Djamila BENNAT

Data sourced from clinicaltrials.gov

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