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Efficacy Study of Minoxidil Lotion Versus Combined Minoxidil and Finasteride Lotion to Treat Male Pattern Hair Loss

Phase 3
Completed
Conditions
Androgenetic Alopecia
Interventions
Registration Number
NCT01391156
Lead Sponsor
Mae Fah Luang University Hospital
Brief Summary

The purpose of this study is to compare the efficacy of 3% Minoxidil lotion and 3% Minoxidil with 0.1% Finasteride lotion for 6 months in male pattern hair loss.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
40
Inclusion Criteria
  • male, age 18-15 years
  • androgenetic alopecia grade 3V to 5 ( Norwood-Hamilton classification)
Exclusion Criteria
  • use minoxidil in 6 months
  • use finasteride in 12 months
  • use ketoconazole, tar, selenium shampoo, topical tretinoin, topical steroid in 2 weeks
  • seborrheic dermatitis or psoriasis on scalp
  • history of allergy to minoxidil, finasteride

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Minoxidil3%Minoxidil lotion-
MinoxidilFinasteride3% Minoxidil with 0.1% Finasteride lotion-
Primary Outcome Measures
NameTimeMethod
The mean change of hair count from baseline and 6 monthsbaseline and 6 months

Total hair count on the vertex is measured on 1 cm2 circular area. The mean change in hair count is compared at baseline and 6 months.The significance of change is determined by Unpaired t Test.

Secondary Outcome Measures
NameTimeMethod
Global photographic assessment by dermatologistsbaseline and 6 months

Photographs of the vertex scalp are taken at baseline and 6 months. A panel of 3 dermatologists assesssed the change in hair growth using a 7-point scale.

Trial Locations

Locations (1)

Mae Fah Luang University Hospital(Bangkok)

🇹🇭

Bangkok, Thailand

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