About this trial
This phase II trial compares the safety and effectiveness of topical minoxidil alone to topical minoxidil in combination with low-level red-light therapy for improving chemotherapy-induced hair loss or thinning (alopecia). Minoxidil has been approved by the Food and Drug Administration as a treatment for hair loss. It increases blood flow in the skin and may have a direct stimulatory effect on hair follicle cells, forcing them from their resting phase into their active growth phase. Low-level light therapy is regarded as a safe and medically accepted treatment for a variety of skin conditions, including acne, scars, and psoriasis. Red light wavelengths are readily absorbed into the skin and do not contain harmful ultraviolet light. When absorbed into the skin, these wavelengths stimulate fibroblasts, which are connective tissue cells that make and secrete collagen proteins. Low-level red-light therapy may improve hair loss by stimulating hair follicles. Combining minoxidil with low-level red-light therapy may be safe and more effective at improving chemotherapy-induced alopecia than minoxidil alone.
Eligibility criteria
Qualifiers
Patients will be Ohio State University patients > 18 years old
Patients will have a diagnosis of breast cancer, stages I-IV
Patients will have been treated with a chemotherapy regimen containing either an anthracycline or taxane
Patients will have a loss of at least 50% of the hair on the scalp by the final chemotherapy infusion
Disqualifiers
None
Trial design
Treatments tested in this trial
- Electronic Health Record Review
- Minoxidil
- Revian RED LED-light cap
- Survey Administration