Prospective Perioperative Clinical Registry for Women Undergoing Benign Gynecological Surgery

Sponsor
IRCCS San Raffaele
Study ID
NCT07772076
Status
Not Yet Recruiting

Notify me when recruiting opens

Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.

Not yet recruiting

Add your contact details and location so we can keep your interest tied to this study.

Conditions

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

Eligibility Criteria

Sex
FEMALE
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Standard Surgical Procedures for Benign Gynecological Conditions — PROCEDURE
    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.

Study Details

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.

Key Dates

First listed
Aug 19, 2026
Start date
Sep 30, 2026
Status verified
Aug 2026
Primary completion
Sep 30, 2036
Completion
Sep 30, 2039

Study Design

Enrollment
6,000 participants (estimated)

Arms

  • Arm: Gynecological Surgery Cohort
    Women with indication for elective benign gynecological surgery undergoing standard clinical surgical procedures (laparoscopy, laparotomy, vaginal, robotic, hysteroscopy, vNOTES).

Primary Outcome Measure

Intraoperative and Postoperative Complications [ Time Frame: perioperatively/periprocedurally ]

Central Contacts

Find similar trials

Nationwide
Endometriosis trialsWomen's health trialsFertility trials

Related Studies