MedTrace Logo

Efficacy and Safety of 3% Minoxidil Lotion for Beard Enhancement

NCT02275832 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 48

Last updated 2015-04-22

No results posted yet for this study

Summary

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

Conditions

  • Beard Enhancement

Interventions

DRUG

3 % Minoxidil lotion

DRUG

Placebo

Sponsors & Collaborators

  • Mae Fah Luang University Hospital

    lead OTHER

Principal Investigators

  • Chuchai Tanglertsampan, MD · MFL University Hospital (Bangkok)

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-11-30
Primary Completion
2015-03-31
Completion
2015-03-31

Countries

  • Thailand

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02275832 on ClinicalTrials.gov