This is a multicentre, open label, randomized, pilot study to evaluate safety and efficacy of Human Platelet Lysate (HPL) in subjects with Androgenetic Alopecia undergoing hair transplantation. The study is being conducted at 2 centers in India. The primary endpoints are Increase in Hair Follicle viability after transplant, Improvement in Caliber \& Density of hair and Improvement in Photographic assessment from randomization to end of study. The secondary endpoints are Physicians and Patients self assessment score.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Study arm A subjects will receive hair follicles transplants that are dipped in HPL before transplant
Study arm B subjects will receive hair follicles transplants that are dipped in HPL before transplant; followed by one HPL injection
Control arm subject will receive Standard hair follicle transplant
Kasiak Research Pvt Ltd
Thane, Maharashtra, India
Improvement in Calibre & Density of Hair as assessed by Folliscope
Time frame: Day 0, Month 2, End of Study - Month 4
Photographic assessment
Time frame: Day 0, Month 1, Month 2, Month 3, End of Study - Month 4
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