Actively Recruiting
In Vivo Treatment Verification of Brachytherapy
Led by Maastricht Radiation Oncology · Updated on 2025-05-09
100
Participants Needed
1
Research Sites
100 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
In Vivo Treatment Verification of Brachytherapy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Treatment site Gynaecology (Endometrium/Cervix) and prostate
- Treatment: HDR Brachytherapy
- Patient will be treated on CT Couch
- Mentally competent patient
You will not qualify if you...
- Incapacitated patient
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Maastro
Maastricht, Limburg, Netherlands, 6229 ET
Actively Recruiting
Research Team
J
Janneke Waelen
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
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