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NCT07772076Not yet recruiting

Prospective Perioperative Clinical Registry for Women Undergoing Benign Gynecological Surgery

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

Source: ClinicalTrials.gov · Last updated 19 Aug 2026

Brief summary (registry, in English)

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.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
6000 (estimated)
First submitted
3 Aug 2026
Start date
Sept 2026
Primary completion date
Sept 2036
Lead sponsor
IRCCS San Raffaele
NCT number
NCT07772076

What you commit to

  • Study type: Observational
  • Planned participants: 6000
  • From Sept 2026 to the primary completion date, Sept 2036
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Emergency / unscheduled surgical procedure
  • No indication for surgery

Other illness

  • Suspected or confirmed malignant gynecological disease

Age

  • Age \< 18 years

Other

  • Current pregnancy
  • Refusal or inability to provide signed informed consent

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
IRCCS Ospedale San Raffaele - U.O. Ginecologia e Ostetricia
Coordinator of this site? Confirm its status
MilanItalyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.