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Minoxidil Response Testing in Females With Female Pattern Hair Loss

NCT02206802 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2018-10-05

No results posted yet for this study

Summary

The primary purpose of this study is to evaluate the clinical validity of the minoxidil response in-vitro diagnostic kit.

Conditions

Interventions

DRUG

5% minoxidil topical foam

5% minoxidil topical foam

Sponsors & Collaborators

  • Applied Biology, Inc.

    lead INDUSTRY

Principal Investigators

  • Sharon Keene, MD · Physicians Hair Institute

  • Flavio Grasso, MD · Istituto Medico Tricologico/Studi Life Cronos

  • Rodney Sinclair, MD · Sinclair Dermatology

  • Rachita Dhurat, MD · LTM Medical College & Hospital

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-07-31
Primary Completion
2018-10-31
Completion
2018-10-31

Countries

  • United States
  • Australia
  • India
  • Italy

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 NCT02206802 on ClinicalTrials.gov