In Vivo Treatment Verification of Brachytherapy
To acquire data during High Dose Rate (HDR) brachytherapy treatments aiming to track the brachytherapy source inside the patient verifying the delivery of the treatment plan. Medical images (CT,MRI and US) combined with software developed by the investigator will be employed to predict the response of the Investigation
| Condition(s) | Brachytherapy |
|---|---|
| Status | Recruiting |
| Study type | Observational |
| Summary | To acquire data during High Dose Rate (HDR) brachytherapy treatments aiming to track the brachytherapy source inside the patient verifying the delivery of the treatment plan. Medical images (CT,MRI and US) combined with software developed by the investigator will be employed to predict the response of the Investigational product during the treatment and will be used as reference.The IP will be placed on the side of the treatment table and will acquire data during the whole treatment, which will be compared against information derived from the treatment plan. The IP based method can detect errors and information about motion and treatment uncertainties that are not currently available. |
| Who can participate | Inclusion Criteria: * Treatment site Gynaecology (Endometrium/Cervix) and prostate * Treatment: HDR Brachytherapy * Patient will be treated on CT Couch * Mentally competent patient Exclusion Criteria: * Incapacitated patient |
| Sex | All |
| Lead sponsor | Maastricht Radiation Oncology |
| Locations | Maastricht, Limburg, Netherlands |
| Start date | 2024-02-29 |
| NCT ID | NCT06240559 |
| Official listing | https://clinicaltrials.gov/study/NCT06240559 |