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Clinical Trial Summary

An open label, pilot study involving the use of low dose oral minoxidil to treat permanent chemotherapy-induced alopecia.


Clinical Trial Description

Patients will be evaluated through clinical assessment, histology, quality of life assessment, and adverse event monitoring. The data gathered from this study will be used to determine the safety and efficacy of the treatment regimen for this subset of CIA patients. The oral minoxidil regimen will be considered effective if significant clinical regrowth, positive histological changes, and improved Quality of Life are reported after the onset of treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03831334
Study type Interventional
Source Northwestern University
Contact
Status Active, not recruiting
Phase Early Phase 1
Start date April 9, 2019
Completion date June 2024