This study aims to determine the rate of recurrence of central pelvic organ prolapse in patients who have undergone surgery (sacropexy with and without mesh) for the same pathology.
There is a lack of data in the literature comparing sacroplexing with the use of mesh with sacroplexing performed without the use of mesh in terms of recurrence, improvement in symptoms, and restoration of normal pelvic organ prolapse relationships. The objective of this study is to determine the rate of recurrence of central pelvic organ prolapse in patients with a clinical diagnosis of genital prolapse stage ≥ 2 according to the POP-Q classification who underwent laparoscopic sacroplasty with mesh (group 1) and without mesh (group 2). The study may provide information on the impact of mesh in laparoscopic surgery for the correction of central pelvic organ prolapse.
Study Type
OBSERVATIONAL
Enrollment
160
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Bologna, Bologna, Italy
RECRUITINGAzienda Ospedaliera Universitaria Integrata di Verona
Verona, Verona, Italy
NOT_YET_RECRUITINGRecurrence rate of central pelvic organ prolapse
The rate of recurrence of central pelvic organ prolapse in patients with a clinical diagnosis of genital prolapse stage ≥ 2 according to the POP-Q classification, undergoing sacroplasty with and without mesh
Time frame: 24 months after surgery
Recurrence rate of central pelvic organ prolapse in laparoscopic sacral hysteropexy, sacralcervicopexy and sacralcolpopexy
The rate of pelvic organ prolapse recurrence in patients treated with mesh (group 1) and without (group 2) in the laparoscopic sacral hysteropexy, sacralcervicopexy and sacralcolpopexy
Time frame: 24 months after surgery
Rate of intraoperative and postoperative complications
Evaluation of intraoperative and postoperative complications according to the Clavien-Dindo classification
Time frame: During surgery and within 30 days
Modification of symptoms after surgery
Change in pre- and post-operative symptomatology assessed through the completion of a questionnaire
Time frame: Before surgery and 24 months after surgery
Changes in the disease framework
Change in the disease framework of pelvic organ prolapse according to the POP-Q classification assessed before and after surgery
Time frame: Before surgery and 24 months after surgery
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