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Testing a WearabLE Artificial Intelligence-POwered Device For OPtimal DAily RaDiation Therapy Using Image Guidance
Sponsor: Medical College of Wisconsin
Summary
This is a device feasibility study to determine the feasibility of automatically predicting time to treatment readiness using a wearable imaging device (Fullyet) in both healthy volunteers and patients with pelvic malignancies undergoing radiation therapy.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
15
Start Date
2025-05-02
Completion Date
2026-10-30
Last Updated
2026-09-15
Healthy Volunteers
Yes
Conditions
Interventions
Fullyet Device and CT Scans
Cancer patients will wear the Fullyet Device. Real-time data will go to the patient and radiation therapy team. When the Fullyet Device indicates that the bladder is at optimal size, the radiation oncology team will get the patient. The patient will then have a CT scan.
Fullyet Device and MRI Scans
Healthy volunteers will first have an MRI scan. Then, they will wear the Fullyet Device. They will have up to two more MRIs to confirm bladder volume.
Locations (1)
Froedtert & the Medical College of Wisconsin
Milwaukee, Wisconsin, United States