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Safety & Effectiveness of the BEAM Device in Mild-to-moderate Acne

NCT01162837 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 33

Last updated 2012-05-03

No results posted yet for this study

Summary

This study will determine if the use of the BEAM device reduces the signs and symptoms of mild-to-moderate acne.

Conditions

Interventions

DEVICE

BEAM device

A red/blue LED device for the treatment of acne

Sponsors & Collaborators

  • Oregon Aesthetic Technologies

    lead INDUSTRY

Principal Investigators

  • Ben Ehst, MD · Oregon Health and Science University

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
15 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-06-30
Primary Completion
2010-09-30
Completion
2010-10-31

Countries

  • United States

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 NCT01162837 on ClinicalTrials.gov