CompletedEarly Phase 1NCT06748287

A Clinical Comparison of FDA-Cleared Photobiomodulation Devices for the Treatment of Alopecia

Studying Alopecia

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Key facts

Sponsor
University of Minnesota
Principal Investigator
Maria K Hordinsky, MD
University of Minnesota
Intervention
iGrow Hair Growth System(device)
Enrollment
104 target
Eligibility
21-85 years · All sexes
Timeline
20172023

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 NCT06748287 on ClinicalTrials.gov

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