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The primary objective of this study is to compare 30-day complication rates associated with promontofixation for pelvic organ prolapse performed via a robot-assisted laparoscopic technique versus a no...
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Lead Sponsor
Centre Hospitalier Universitaire de Nīmes
NCT04829058 · Pelvic Organ Prolapse
NCT05602246 · Pelvic Organ Prolapse, Cystocele, and more
NCT07150442 · Pelvic Organ Prolapse Vaginal Surgery, Platelet Rich Plasma Injection
NCT06461234 · Pelvic Floor Disorders, Pelvic Organ Prolapse
NCT06802497 · Pelvic Organ Prolapse
CHU de Nîmes - Hôpital Universitaire Carémeau
Nîmes, Gard
Groupe Urologie Saint Augustin
Bordeaux
APHP - Centre Hospitalier Henri Mondor
Créteil
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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.
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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