Ireland
--:--IST
Recruiting Observational

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

NCT05102240 · tracked via the Priya Life Science India tracker
Phase
Observational
Started
2022-02-24
Last updated
2026-02-20

Condition(s) studied

Cervix Cancer

Study summary

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.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
90 Years
Healthy volunteers
No
Inclusion Criteria: For Aim 1 and Aim 3: * 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 For Aim 2 * Patients undergoing postoperative or definitive radiotherapy and treated within trials of postoperative or definitive RT. Exclusion Criteria: 1. Lack of disease or toxicity outcomes. 2. Lack of images in the hospital database.

Primary outcome measure(s)

  • Generation of software for automated target delineation for cervix cancer — 3 years
    1\. To develop and validate automated platforms for target delineation and planning for cervix cancer in time efficient manner through a. Machine learning based detection of abnormal cancerous tissues in multimodality medical diagnostic images. b . To train machine base systems for automated planning of external radiation and brachytherapy for gynaecological cancers.
  • Development and validation of Normal Tissue Complication Plots — 3 years
    2\. To use existing databases and radiation dose maps, imaging texture features and adverse events data for machine learning to develop "normal tissue complication plots "and to identify cervix cancer patient subgroups that may benefit from advanced radiation techniques (like proton treatment)
  • Identify "high risk patient population" that may benefit from intensification of treatment in future — 3 years
    3\. To use advanced image texture analysis within ongoing institutional and collaborative clinical trials to identify "high risk patient population" that may benefit from intensification of treatment in future

Trial sites (1)

FacilityCityRegionStatus
Advanced Centre of Treatment Research and Education In Cancer,Tata Memorial Centre Navi Mumbai Maharashtra Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05102240 on ClinicalTrials.gov ↗ ← All trials in India