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Collects clinical data on women having surgery for benign gynecological conditions

Records data before, during and after surgery for benign gynecological conditions in adult women.

Plain-language title generated from the registry record
Registry title: Prospective Perioperative Clinical Registry for Women Undergoing Benign Gynecological Surgery

Key facts

Where
Milan, ItalySee the site

Where in Italy

  • IRCCS Ospedale San Raffaele - U.O. Ginecologia e OstetriciaMilan, ItalyNo longer taking part

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Trial details

Who runs it
IRCCS San Raffaele
Trial code
NCT07772076
Record updated
19 August 2026
Original description
This prospective observational registry aims to systematically collect preoperative, intraoperative, and postoperative clinical data from patients undergoing surgery for benign gynecological conditions. The main goal is to evaluate clinical outcomes, surgical approaches, and complications in real-world clinical practice.Read full original descriptionShow less

Prospective Observational Registry on the Collection of Perioperative Clinical Data in Gynecology

This prospective observational registry aims to systematically collect preoperative, intraoperative, and postoperative clinical data from patients undergoing surgery for benign gynecological conditions. The main goal is to evaluate clinical outcomes, surgical approaches, and complications in real-world clinical practice.

Inclusion: Age >= 18 years; Diagnosis of benign gynecological disease (e.g., uterine fibroids, endometriosis, pelvic neoplasm, endometrial polyp, endometrial hyperplasia, cervical dysplasia, pelvic adhesions, isthmocele, genital prolapse, adenomyosis, female genital malformations, pelvic inflammatory disease); Indication for elective benign gynecological surgery; Signed written informed consent for data collection.

Exclusion: Emergency / unscheduled surgical procedure; No indication for surgery; Suspected or confirmed malignant gynecological disease; Age < 18 years; Current pregnancy; Refusal or inability to provide signed informed consent.

ClinicalTrials.gov NCT07772076