Actively Recruiting

Age: 18Years - 90Years
FEMALE
NCT05102240

Development of Clinically High Efficient Platforms for Individualised Treatment of Cervix Cancer

Led by Tata Memorial Hospital · Updated on 2026-02-20

1800

Participants Needed

1

Research Sites

226 weeks

Total Duration

On this page

Sponsors

T

Tata Memorial Hospital

Lead Sponsor

B

Bhabha Atomic Research Centre

Collaborating Sponsor

AI-Summary

What this Trial Is About

Retrospective study utilizing patient data to develop and validate Machine Learning application. Available imaging data sets of patients who have completed treatment will be used to develop Normal tissue complication probability and Tumour control probability Hypothesis Integrating existing radiation treatment information, quantitative imaging and patient outcome data from completed and ongoing clinical trials will allow development of knowledge based systems for efficient treatment delivery and allow selection of patients for intensified treatment approaches in cervix cancer.

CONDITIONS

Official Title

Development of Clinically High Efficient Platforms for Individualised Treatment of Cervix Cancer

Who Can Participate

Age: 18Years - 90Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients treated within ongoing and completed clinical trials of chemoradiation and brachytherapy for cervix cancer with access to MRI/CT images at the time of diagnosis and brachytherapy
  • Patients undergoing postoperative or definitive radiotherapy and treated within trials of postoperative or definitive radiotherapy
Not Eligible

You will not qualify if you...

  • Lack of disease or toxicity outcomes
  • Lack of images in the hospital database

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Advanced Centre of Treatment Research and Education In Cancer,Tata Memorial Centre

Navi Mumbai, Maharashtra, India, 410210

Actively Recruiting

Loading map...

Research Team

S

Supriya Sastri (nee Chopra), MD

CONTACT

S

Supriya Sastri (nee Chopra), MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here