Infrared Non-Cutting Laser Therapy for Acne

Completed · Phase 2/Phase 3

Conditions studied: Acne Vulgaris

In brief

The purpose of this research project is to study the effect of non-ablative (non-cutting) laser therapy, a technique that uses laser energy to try to improve the appearance of the skin. In this study, we are interested in learning how well such a laser works to improve the symptoms of acne. The laser used in this particular study will be the CoolTouch II® laser, manufactured by ICN Photonics, Inc., and has not been FDA-approved for the treatment of acne.

Key facts

Study ID

NCT00110643

Run by

University of Michigan

People needed

50

Starts

2003-02-01

Expected to finish

2005-12-01

Last updated by the study team

2015-05-04

Who can join

Age: 13 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age 13 years or older of either gender and of any racial/ethnic group.
• Subjects must have clinically evident acne vulgaris of the facial skin.
• Subjects must understand and sign the informed consent prior to participation.
• Subjects must be in generally good health.
• Subjects must be able and willing to comply with the requirements of the protocol.
• You must live within a reasonable driving distance of Ann Arbor, Michigan, and/or be able to attend all of the scheduled appointments during the study.

You may not qualify if…

• Oral retinoid (Accutane) use within 1 year of entry into the study.
• Systemic acne therapies (oral antibiotics) within 4 weeks of entry into the study.
• Topical acne therapies (retinoids, antibiotics) within 2 weeks of entry into the study.
• Microdermabrasion or superficial chemical peels at the sites to be treated within 3 months of entry into the study.
• Subjects with a history of dermabrasion or laser resurfacing at the sites to be treated.
• Use of topical lipid absorbing substances (Clinac AC) within 2 weeks of entry into the study.
• Non-compliant subjects.
• Subjects with a significant medical history or concurrent illness/condition which the investigator(s) feel is not safe for study participation.
• Subjects using alcohol-based topical solutions or "exfolliating" agents within 2 weeks of entry into the study.
• Subjects with a history of very frequent herpes simplex infections of the face or with clinical evidence of active herpes simplex infections.
• History of keloid scar formation for subjects undergoing biopsies.
• Pregnant or nursing females.

Where it is running

• University of Michigan Dermatology Department — Ann Arbor, Michigan, United States

Full record on ClinicalTrials.gov

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