Skip to main content
OpenTrials
Completed

NCT Number: NCT01160757

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

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

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Arizona State University, College of Nursing and Healthcare Innovation

Phoenix, Arizona, 85004, United States

About this study

Acne vulgaris is a disease that occurs when oil and dead skin cells clog the pores of the skin. When the skin's pores are clogged, red spots and bumps known as pimples are formed, usually on the face, neck, chest, and back. In adolescents and adults, acne vulgaris is commonly called "acne." Many factors have been associated with acne. One of the factors is the increased production of fatty substances from an enlarged sebaceous gland ("oil gland").

The experimental ultrasonic device uses sound waves (called ultrasonic waves) to heat the acute acne lesion and the surrounding sebaceous ("oil") glands deep in the skin without affecting the surface of the skin. We hope that heating the sebaceous glands will reduce their size and reduce the symptoms of inflamed acne. Using ultrasonic waves to treat acne is investigational.

This is a pilot study. A pilot study is done on a small group of subjects to learn if the device will be effective and safe, before the device is used on a larger group of subjects.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • female or male subjects,
  • greater than 18 years age,
  • with acute acne on the face.

Exclusion criteria

  • pregnancy,
  • concomitant skin diseases,
  • severe acne,
  • antibiotic therapy.

Treatment and study plan

Ultrasound

Device

ultrasound exposure on acute acne lesions

Primary outcomes

  1. Time to clear acute acne lesions

    Time frame: 12 days

Sponsors and collaborators

Lead sponsor

Arizona State University

Other

Registry information

Important dates

Study start
2008
Primary completion
2009
First posted
Jul 12, 2010
Registry last updated
Jul 12, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.