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Comparison of Topical Minoxidil 5% in Ethanol Plus Propylene Glycol Versus Minoxidil 5% in Ethanol Alone in Treatment of Women With Female Pattern Hair Loss

NCT04090801 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2019-09-26

No results posted yet for this study

Summary

The study will be included 60 women with FPHL. The diagnosis of FPHL will be established by clinical (Ludwig classification) and trichoscopic evaluation of frontal and occipital regions of the scalp.

Conditions

  • Female Pattern Hair Loss

Interventions

DRUG

Topical minoxidil 5% in 90% ethanol and 5% propylene glycol

DRUG

Topical minoxidil 5% in pure ethanol alone

The treatment will be continued twice daily.for six months with regular visits at 3 months intervals.

OTHER

Placebo (Ethanol)

The treatment will be continued twice daily.for six months with regular visits at 3 months intervals.

Sponsors & Collaborators

  • Sohag University

    lead OTHER

Principal Investigators

  • Mohammed Abu El-Hamd, MD · Faculty of Medicine, Sohag University, Egypt.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
60 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-05-30
Primary Completion
2016-05-30
Completion
2017-01-23

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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 NCT04090801 on ClinicalTrials.gov