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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...
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Lead Sponsor
University Hospital, Clermont-Ferrand
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
NCT07267377 · Cognitive Recovery, Sedation, and more
CHU de Clermont-Ferrand
Clermont-Ferrand
CH d'Issoire
Issoire
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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.
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