Minoxidil 1% for Eyebrow Enhancement

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-12-31

Study Completion Date

2014-04-30

Brief Summary

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The purpose of the study is to compare efficacy and safety of minoxidil 1% versus placebo in enhancement of eyebrows.

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Detailed Description

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Conditions

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Eyebrow Hypotrichosis Thin Eyebrow

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

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Minoxidil lotion 1%

Minoxidil lotion 1% is applied twice daily to one eyebrow.

Group Type EXPERIMENTAL

Minoxidil lotion 1%

Intervention Type DRUG

Minoxidil lotion 1% is applied twice daily to one eyebrow.

Placebo

Placebo is applied twice daily to the other eyebrow.

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DRUG

Interventions

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Minoxidil lotion 1%

Minoxidil lotion 1% is applied twice daily to one eyebrow.

Intervention Type DRUG

Placebo

Intervention Type DRUG

Other Intervention Names

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Placebo is applied twice daily on the other eyebrow.

Eligibility Criteria

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Inclusion Criteria

* male or female aged 18-60 years
* hypotrichosis of eyebrows
* healthy
* informed consent obtained

Exclusion Criteria

* underlying diseases
* alopecia areata or trichotillomania
* thyroid diseases
* pregnancy or breast feeding
* previous eyebrow tattoo, trauma or accident.
* history of eyebrow or hair medications in 6 months
* history of minoxidil or its ingredient allergy
* history of eyebrow surgery.

Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes