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RECRUITING
NCT06820385
NA

Testing a WearabLE Artificial Intelligence-POwered Device For OPtimal DAily RaDiation Therapy Using Image Guidance

Sponsor: Medical College of Wisconsin

View on ClinicalTrials.gov

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

Interventions

DEVICE

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.

DEVICE

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