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A Novel Approach to Treating Androgenetic Alopecia in Females With Low Level Laser Therapy

NCT01967277 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 44

Last updated 2015-05-06

Study results available
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Summary

This study will acquire data on hair growth of the head that is the result of treatment with a non-heat generating, laser product. This data will come from counting of terminal hairs before treatment begins and after treatment is completed. The treatment regime is every other day for 16 weeks.

Conditions

Interventions

DEVICE

Handi-Dome Laser

One, 30 minute treatment, every other day for 16 weeks.

DEVICE

Incandescent red light source.

One, 30 minute treatment, every other day for 16 weeks.

Sponsors & Collaborators

  • Capillus, LLC

    lead INDUSTRY

Principal Investigators

  • Raymond R. Blanche, BA · NST Consulting, LLC

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2014-03-31
Primary Completion
2014-08-31
Completion
2014-09-30

Countries

  • United States

Study Locations

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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 NCT01967277 on ClinicalTrials.gov