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

Recruitingn/aAges 18 Years - 90 YearsFemaleTata Memorial Hospital
NCT05102240 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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.

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📋 Eligibility rules (as published)
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.
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What it tests

  • Not listed
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Where

1 site
Advanced Centre of Treatment Research and Education In Cancer,Tata Memorial Centre
Navi Mumbai, India
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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