Loading clinical trials...
Loading clinical trials...
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 n...
Keep your clinical trial research organized — questions to ask, what to expect, and key details.
Lead Sponsor
University Hospital, Clermont-Ferrand
NCT07506798 · Gynecologic Surgery, Postoperative Recovery, and more
NCT07264855 · Postoperative Pain, Laparoscopic Gynecologic Surgery
NCT05526534 · Gynecologic Surgery, High-flow Nasal Cannula, and more
NCT07114965 · Postoperative Pain, Gynecologic Surgery
NCT07251101 · Anesthesia, Intravenous, Hemodynamic Stability, and more
CHU de Clermont-Ferrand
Clermont-Ferrand
CH d'Issoire
Issoire
Use Clareo to keep notes, questions, trial details, and next steps organized before and after appointments.
Start free trial →Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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.
View ClinicalTrials.gov Terms and Conditions