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A Study to Determine the Safety and Efficacy of an Ultrasound Device in the Management of Acute Acne Lesions

NCT01160757 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 35

Last updated 2010-07-12

No results posted yet for this study

Summary

The purpose of this study is to find out how effective and safe an experimental ultrasound device is for treating Acute Acne lesions.

Conditions

  • Acne Vulgaris

Interventions

DEVICE

ultrasound

ultrasound exposure on acute acne lesions

Sponsors & Collaborators

  • Arizona State University

    lead OTHER

Principal Investigators

  • Denise Link, PhD · ASU, College of Nursing and Healthcare Innovation

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-10-31
Primary Completion
2009-07-31

Countries

  • United States

Study Locations

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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 NCT01160757 on ClinicalTrials.gov