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TUbal LIgation Per Differents Endoscopic Routes and Sexuality (TULIPES) | Clinical Trials | Clareo Health

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TUbal LIgation Per Differents Endoscopic Routes and Sexuality (TULIPES)

Sexuality After Tubal Sterilization by Conventional Abdominal Laparoscopy or Vaginal Natural Orifice Transluminal Endoscopy (vNOTES) : a Randomised Controlled Trial

NCT05910385•University Hospital, Clermont-Ferrand

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is compare the quality of sexual life at 6 months after tubal ligation, depending on whether it was performed by abdominal laparoscopy or by vNOTES, on the basis of a non-inferiority hypothesis. Participants will answer on the FSFI-19 questionnaire and quality of sexual life will be evaluated according to the score obtained at 6 months post-operative compared to pre-operative.

Eligibility

Age

18 - No limit years

Sex

FEMALE

Healthy Volunteers

Inclusion Criteria

•Adult woman, eligible for tubal ligation by total salpingectomy or tubal section coagulation, sexually active at the time of inclusion
•Able to give informed consent to participate in research
•Affiliated to a social security system.

Exclusion Criteria

•Current pregnancy or breastfeeding
•Indications of another concomitant surgical procedure (other than procedure on the appendix)
•History of upper genital infection
•Proven or suspected rectovaginal endometriosis on clinical examination
•History of rectal surgery
•Virgin patient
•Any concomitant pathology deemed incompatible with the study.
•Uncured COVID or SARS-COv2 positivity dated less than 3 days prior to surgery.
•Protected adult patient, under guardianship or curatorship
•Patients not affiliated to the social security system
+3 more criteria

Locations (2)

CHU de Clermont-Ferrand

Clermont-Ferrand, France

CH d'Issoire

Issoire, France

Key Dates

Start Date

May 23, 2022

Primary Completion Date

November 18, 2025

Completion Date

November 18, 2025

Last Updated

December 1, 2025

Enrollment

140

ACTUAL participants

Conditions

Gynecologic Surgery

Interventions

laparoscopy

PROCEDURE

vnotes

PROCEDURE

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: December 1, 2025Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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TUbal LIgation Per Differents Endoscopic Routes and Sexuality (TULIPES)

Inclusion Criteria

Exclusion Criteria

A RCT on the Preventive Effect of HFNC on Postoperative Pulmonary Complications in Patients With Gynecologic Neoplasms

Effects Of Quadratus Lumborum Type 1 Block And Transversalis Facial Plane Block On Acute Pain In Gynecological Surgery

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Hemodynamic Effects of Remimazolam vs Propofol During Robot-assisted Gynecologic Surgery

Long-term Follow-up of Bio-signals and Quality of Recovery Following Implementation of ERAS

Comparison Volume-controlled Ventilation, Pressure-controlled Volume-guaranteed Ventilation, and Pressure-controlled Ventilation During Gynecologic Laparoscopic Surgery in the Steep Trendelenburg Position