RecruitingNot applicableNCT07535541

A Feasibility Study of Biometric Measurements Via Wearable Smart Watch Technology for Evaluation of Vasomotor Symptoms in Patients Treated With Androgen Deprivation Therapy for Prostate Cancer (Prostate 007)

Studying Epilepsy with eyelid myoclonia

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Key facts

Sponsor
University of Virginia
Principal Investigator
Michael Devitt, MD, M.D
University of Virginia
Intervention
VMS logging(behavioral)
Enrollment
18 target
Eligibility
18 years · MALE
Timeline
20262027

Study locations (1)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT07535541 on ClinicalTrials.gov

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