Development of Clinically High Efficient Platforms for Individualised Treatment of Cervix Cancer
NCT05102240
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
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.
Conditions2
Browse More Trials
Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
This site does not provide medical advice. Always consult your doctor before considering enrollment in a clinical trial. Learn more on our About page.
NCT05102240