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vNOTEsHC : Hysterectomy by transvaginal natural orifice transluminal endoscopic surgery versus laparoscopic for large uteri: study protocol for a multicentre randomised controlled trial

BACKGROUND: In France, 62,000 hysterectomies are performed per year, 70% of which are benign. The choice of approach (laparotomy, laparoscopy or vaginal route) is particularly important in the case of large uterus (> 280g) which are associated with a higher risk of complications. The current data...

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Detalles Bibliográficos
Autores principales: Druenne, J, Presles, E, Corsini, T, Campagne Loiseau, S, Curinier, S, Mansour, A, Lamblin, G, Reboul, Q, Chauleur, C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Universa Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10643007/
https://www.ncbi.nlm.nih.gov/pubmed/37742205
http://dx.doi.org/10.52054/FVVO.15.3.083
Descripción
Sumario:BACKGROUND: In France, 62,000 hysterectomies are performed per year, 70% of which are benign. The choice of approach (laparotomy, laparoscopy or vaginal route) is particularly important in the case of large uterus (> 280g) which are associated with a higher risk of complications. The current data are not sufficient to favour one or other approach. A new medical device, the vNOTES (Natural Vaginal Orifice Transluminal Endoscopy System), offers the advantage of both laparoscopic and vaginal route for pelvic surgery. OBJECTIVES: To demonstrate the superiority in terms of intraoperative and postoperative complications of the use of a natural orifice transluminal endoscopic hysterectomy system (vNOTES) versus laparoscopic hysterectomy for benign pathologies on estimated large volume uteri (>280g) MATERIALS AND METHODS: A randomised, double-blind, superiority trial will be performed at five hospital centres. Women with benign uterine pathology requiring hysterectomy and with a large uterus (> 280g) will be randomised to receive either laparoscopic or vNOTES hysterectomy. MAIN OUTCOME MEASURES: The primary outcome will be the occurrence of intraoperative and postoperative complications within 6 weeks of surgery. Secondary outcomes will be conversion during surgery, duration of surgery and hospitalisation, postoperative pain, postoperative complications, resumption of sexual life and satisfaction with the surgical team. RESULTS: 248 women will be randomised. CONCLUSION: This trial will provide a better understanding of the approach to large uteri optimise the care of these thousands of women undergoing hysterectomy. WHAT'S NEW? This trial will evaluate the vNotes for large uteri.