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A Prospective, Multicentric, Open Label, Bio Interventional, Phase I, Phase II Pilot Study to Evaluate the Safety and Efficacy of Autologous Human Platelet Lysate (HPL) for Treatment of Acne Scarring

NCT01644435 Phase 1/Phase 2 COMPLETED

This is a multicentre, open label, randomized, pilot study to evaluate safety and efficacy of Human Platelet Lysate (HPL) in subjects with Acne Scarring. The study is being conducted at 2 centers in India. The primary endpoint is change in the Global Acne scarring classification scores from screening to end of the study. The secondary endpoints are Photographic Assessment, Physicians assessment score and Patients self assessment score.

Details

Lead sponsorKasiak Research Pvt. Ltd.
PhasePhase 1/Phase 2
StatusCOMPLETED
Enrolment19
Start date2012-05
Completion2012-10

Conditions

Interventions

Primary outcomes

Countries

India