Efficacy and Safety of 3% Minoxidil Lotion for Chest Hair Enhancement

Phase 4

• Conditions: Chest Hair Enhancement
• Interventions: Drug: 3 % minoxidil lotion; Drug: Placebo

• Registration Number: NCT02283645
• Lead Sponsor: Mae Fah Luang University Hospital

Brief Summary

The purpose of this study is to determine efficacy and safety of 3% minoxidil lotion for chest hair enhancement.

Detailed Description

Not available

Study Timeline

• Status Verified: 2014-11
• Study First Submitted: 2014-11-02
• Study First Submitted QC: 2014-11-04
• Study First Posted: 2014-11-05
• Last Update Submitted: 2014-11-29
• Last Update Posted: 2014-12-02
• Study Start: 2015-01
• Primary Completion: 2015-08
• Study Completion: 2015-08

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: Male
• Target Recruitment: 64

Inclusion Criteria

• healthy male

Exclusion Criteria

• serious underlying diseases
• history of chest/ hair treatment before 6 months
• history of surgery or trauma on chest area.
• history of minoxidil allergy

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Minoxidil	3 % minoxidil lotion	3% Minoxidil lotion is applied twice daily to the chest.
Placebo	Placebo	Placebo lotion is applied twice daily to the chest.

Primary Outcome Measures

Name	Time	Method
The change of global photographic assessment after 20 weeks from baseline	baseline and 20 weeks

Secondary Outcome Measures

Name	Time	Method
The change in number of hairs after 20 weeks from baseline	baseline and 20 weeks