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Prospective Perioperative Clinical Registry for Women Undergoing Benign Gynecological Surgery

NCT07772076 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 6000

Last updated 2026-08-19

No results posted yet for this study

Summary

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.

Conditions

  • Benign Gynecological Disease
  • Uterine Fibroids
  • Endometriosis
  • Adenomyosis
  • Pelvic Adhesions
  • Ovarian Cyst Benign
  • Salpingitis
  • Polyp Endometrium
  • Ectopic Pregnancy

Interventions

PROCEDURE

Standard Surgical Procedures for Benign Gynecological Conditions

Patients undergo standard-of-care elective surgery for benign gynecological conditions according to routine clinical practice, including laparoscopy, laparotomy, vaginal surgery, robotic-assisted surgery, operative hysteroscopy, or vNOTES. The choice of procedure is determined solely by clinician judgment and standard medical indication. Data on surgical technique, intraoperative parameters, and perioperative outcomes are recorded prospectively.

Sponsors & Collaborators

  • IRCCS San Raffaele

    lead OTHER

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-09-30
Primary Completion
2036-09-30
Completion
2039-09-30

Countries

  • Italy

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07772076 on ClinicalTrials.gov