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NCT07354087Active, not recruiting

Impact of Molecular Pathological And Clinical Features for Adjuvant Treatment Selection in Endometrial Cancer: Asian Registry

Impact of Molecular Pathological And Clinical Features for Adjuvant Treatment Selection in Endometrial Cancer: Multicentric Asian Registry (IMPACT-Endo-Asia)

Source: ClinicalTrials.gov · Last updated 4 Feb 2026

Brief summary (registry, in English)

The treatment practices for endometrial cancer have significantly changed over the last two decades. Nowadays, in addition to standard pathology, additional tests are performed to understand the behaviour of tumour so that personalized treatment can be advised for every patient. This approach ensures that patients with good cancer cell features receive minimum essential radiotherapy or surgery treatment with fewer side effects, while those with poor cell features undergo more aggressive treatment to improve their chances of survival. However, this approach is not widely adopted in Asian countries. To address this, investigators are launching a project to gather data from various hospitals across Asia. The project aims to understand how different cancer cell factors impact treatment decisions and identify better ways to select additional treatment plans based on a patient's cancer cell features. The project will gather data from around 250-300 patients who were evaluated or treated between January 2021 and December 2023. It will run for two years to improve our understanding and gain insights into the best ways to treat endometrial cancer.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
300 (actual)
First submitted
24 Jan 2025
Start date
28 Nov 2024
Primary completion date
27 Nov 2026
Lead sponsor
Tata Memorial Hospital
NCT number
NCT07354087

What you commit to

  • Study type: Observational
  • Participants enrolled: 300
  • From 28 Nov 2024 to the primary completion date, 27 Nov 2026
  • 2 sites 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 illness

  • \- Patients with final histopathological diagnosis of any other gynecological malignancy other than EC and its subtypes.

Who the study is looking for

  • \- Patients who were diagnosed to have EC and have access to standard histopathological reports and availability of treatment decisions.

Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

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

SiteCityCountrySite status
Tata Memorial Hospital
Coordinator of this site? Confirm its status
MumbaiIndiaUnknown status
Advanced Centre for Treatment, Research and Education in Cancer, Tata Memorial Centre
Coordinator of this site? Confirm its status
Navi MumbaiIndiaUnknown status

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