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Clinical Trials/NCT02594046
NCT02594046
Completed
Not Applicable

The Effect of Allogeneic Human Adipose Derived Stem Cell Component Extract on Androgenic Alopecia

Pusan National University Hospital0 sites38 target enrollmentJuly 1, 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Androgenic Alopecia
Sponsor
Pusan National University Hospital
Enrollment
38
Primary Endpoint
change of total hair counts by phototrichogram
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

This randomized, placebo-controlled, double-blind study evaluates the efficacy and tolerability of the allogeneic human adipose derived stem cell component extract on androgenic alopecia in relatively healthy adults. A total of 38 subjects received 1.2 g of allogeneic human adipose derived stem cell component extract per month or a placebo for 16 weeks.

Detailed Description

This randomized, placebo-controlled, double-blind study evaluates the efficacy and tolerability of the allogeneic human adipose derived stem cell component extract on androgenic alopecia in relatively healthy adults. A total of 38 subjects received 1.2 g of allogeneic human adipose derived stem cell component extract per month or a placebo for 16 weeks. Hair count and thickness will be primary outcomes.

Registry
clinicaltrials.gov
Start Date
July 1, 2015
End Date
May 28, 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sang Yeoup Lee

professor

Pusan National University Hospital

Eligibility Criteria

Inclusion Criteria

  • androgenic alopecia basic and specific(BASP) classification: M2, C2, U1, V1, or F1 or higher

Exclusion Criteria

  • patient of scalp disease

Outcomes

Primary Outcomes

change of total hair counts by phototrichogram

Time Frame: 16 weeks

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