Prospective Perioperative Clinical Registry for Women Undergoing Benign Gynecological Surgery

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.

Benign gynecological diseases frequently require surgical intervention via laparoscopy, laparotomy, vaginal, or robotic approaches. This single-center registry prospectively records baseline patient characteristics, surgical parameters, intraoperative complications, and postoperative outcomes up to 30 days post-surgery (with standard clinical follow-up up to 3 years). The collected data will enable descriptive and exploratory comparative evaluations to optimize perioperative care and surgical management.

Inclusion Criteria:

1. Age >= 18 years
2. 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)
3. Indication for elective benign gynecological surgery
4. Signed written informed consent for data collection

Exclusion Criteria:

1. Age < 18 years
2. Suspected or confirmed malignant gynecological disease
3. Current pregnancy
4. Emergency / unscheduled surgical procedure
5. No indication for surgery
6. Refusal or inability to provide signed informed consent