Fact CheckerSign in

NCT07558889Recruiting

The Surveillance, Epidemiology, and End Results Database Program on Endometrial Cancer in the Italian Population

The ENDOCancer-DATA: the Surveillance, Epidemiology, and End Results Database Program on Endometrial Cancer in the Italian Population

Source: ClinicalTrials.gov · Last updated 30 Apr 2026

Brief summary (registry, in English)

The aim of this study is to lay the bases for an ambitious project that reports and records all the epidemiological-clinical information of the cases of endometrial carcinoma diagnosed and treated in the reference oncology centers involved on the national territory, to create a process of analysis of the data

Status (registry)
Recruiting
Study type
Observational
Enrollment
10000 (estimated)
First submitted
19 Mar 2024
Start date
1 Apr 2024
Primary completion date
1 Jan 2029
Lead sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
NCT number
NCT07558889

What you commit to

  • Study type: Observational
  • Planned participants: 10000
  • From 1 Apr 2024 to the primary completion date, 1 Jan 2029
  • 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.

Other

  • patients with missing information
  • patients not treated in the participating centers for which only partial and fragmented information will be available
  • molecular profile not known and\\or not recoverable and retrospectively analysable

Who the study is looking for

  • diagnosis of endometrial cancer (stage I-IV, G1-3, and special histotypes)
  • age \> 18 years
  • American Society of Anesthesiologists classification (ASA score) 1-3
  • patients undergoing staging, cytoreduction or diagnostic surgery with acquisition of histological examination on which IHC and/or NGS studies have been performed for the molecular profile of the carcinoma
  • Signed informed consent

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
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Coordinator of this site? Confirm its status
RomaItalyRecruiting

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