This is a multicentre, open label, randomized, pilot study to evaluate safety and efficacy of Human Platelet Lysate (HPL) in subjects with Androgenetic Alopecia. The study is being conducted at 2 centers in India. The primary endpoints are 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
20
Study arm A will include subjects receiving three doses of Autologous Human Platelet Lysate at an interval of one month each.
Control arm B subjects will receive Standard therapy (2% Minoxidil and/or Finasteride)
Kasiak Research Pvt Ltd
Thane, Maharashtra, India
Change in Calibre & Density of Hair as assessed by Folliscope
Time frame: Day 0, Month 4, End of study - Month 6
Photographic Assessment
Time frame: Day 0, Month1, Month 2, Month 3, Month 4, Month 5, Month 6
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