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The primary purpose is to evaluate the quality of post-operative recovery and post-operative pain in elderly patients (more than 75 years) who undergo laparoscopic surgery for uterine prolapse.
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Lead Sponsor
University Hospital, Clermont-Ferrand
NCT07295782 · Uterine Prolapse, Urine Incontinence
NCT06024109 · Abnormal Uterine Bleeding, Endometriosis, and more
NCT05586984 · Pelvic Organ Prolapse, Uterine Prolapse
NCT06902909 · Vaginal Vault Prolapse, Uterine Prolapse, and more
NCT06524700 · Uterine Prolapse, Vault Prolapse, Vaginal
CHU Clermont-ferrand
Clermont-Ferrand
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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