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Evaluating the Topical Herbal Solution on the Treatment of Male Pattern Hair Loss and Comparison With Minoxidil 5%

NCT03753113 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2020-03-16

Study results available
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Summary

The purpose of this study is evaluating the efficacy and safety of a topical herbal solution in males for the treatment of Androgenetic alopecia.

Conditions

Interventions

DRUG

Topical Herbal Solution

Use Topical Herbal Solution every day in scalp hair loss areas for 36 weeks.

DRUG

Topical Minoxidil 5%

Use Minoxidil 5% solution every day in scalp hair loss areas for 36 weeks.

Sponsors & Collaborators

  • Farid Masoud

    lead OTHER

Principal Investigators

  • Farid Masoud, PharmD · Pharmacy Faculty

  • Yousef Javadzadeh, Ph.D · Department of Pharmaceutics, Pharmacy Faculty

  • Hamideh Azimi Alamdari, MD · Department of Dermatology, Faculty of Medicine

  • Solmaz Asnaashari, Ph.D · Department of Pharmacognosy, Pharmacy Faculty

  • Javad Shokri, Ph.D · Department of Pharmaceutics, Pharmacy Faculty

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2018-11-28
Primary Completion
2019-09-02
Completion
2019-09-02

Countries

  • Iran

Study Locations

More Related Trials

Entities

Diseases

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 NCT03753113 on ClinicalTrials.gov