Non-Cutting Laser Therapy in the Treatment of Acne
This study is currently recruiting patients.
Verified by University of Michigan September 2006
| Sponsored by: |
University of Michigan |
| Information provided by: |
University of Michigan |
| ClinicalTrials.gov Identifier: |
NCT00113425 | |
Purpose
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. This type of laser treatment creates changes in a layer of the skin called the dermis without causing an open wound in the skin. The use of non-ablative laser therapy, together with application of a photo-sensitizer (substance that makes the skin more sensitive to light), may improve the appearance of acne. The idea behind the photo-sensitizer is that it is supposed to make the laser more effective than using just the laser alone. It is not yet clear how much improvement can be seen with these treatments or exactly how the skin’s response causes these improvements. In this study, we are interested in learning how well such a laser works to improve the symptoms of acne, as well as how much the photo-sensitizer actually enhances the efficacy of the laser.
| Condition |
Intervention |
Phase |
Acne Vulgaris
|
Device: V-Beam laser, Candela Corp., 595 nm wavelength
|
Phase II
|
MedlinePlus related topics: Acne
Study Type: Interventional
Study Design: Treatment, Randomized, Single Blind, Active Control, Single Group Assignment, Safety/Efficacy Study
Official Title: Photodynamic Therapy in the Treatment of Acne Vulgaris
Further study details as provided by University of Michigan:
Primary Outcomes: Subtypes of acne lesions including papules, pustules, cysts, open comedones, and closed comedones
Secondary Outcomes: cutaneous sebum production (optional)
Expected Total Enrollment: 75
Study start: August 2005; Expected completion: August 2008
Last follow-up: March 2008; Data entry closure: June 2008
Acne vulgaris remains among the most common cutaneous disorders, impacting the vast majority of people at some point during their lives. It is associated with significant psychosocial morbidity, and there remains the need for efficacious and low risk therapeutic options.
Recently, the FDA has approved various lasers for the treatment of acne. However, few randomized, controlled clinical trials have been performed. In addition, the use of topical photosensitizers preceding laser therapy for acne has also been examined in a preliminary way with some initial evidence of efficacy. However, these small trials have primarily focused on back acne and have included modest numbers of subjects. Photodynamic therapy for facial acne is being performed by physicians across the country but little objective data regarding this practice is available.
We propose to evaluate the efficacy and confirm the safety of pulsed dye laser therapy (V-Beam laser, Candela Corp., Wayland, MA, 595 nm wavelength) used in conjunction with a topical photosensitizer in the treatment of acne vulgaris. This is a split-face comparison study in which one half of the face will be treated with photo-sensitizer and laser, and the contralateral side will be left untreated. Because one proposed mechanism of action for such treatments includes altered sebaceous gland activity, we also seek to examine the effects of this treatment on cutaneous sebum production.
Eligibility
Ages Eligible for Study: 15 Years and above, Genders Eligible for Study: Both
Criteria
Inclusion Criteria:
- Age 15 years or older of either gender and of any racial/ethnic group.
- Presence of clinically-evident facial acne.
- 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.
Exclusion Criteria:
- Oral retinoid (Accutane) use within 6 months 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 2 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 (excessive scar) formation for subjects undergoing biopsies.
- Pregnant or nursing females.
- Subjects with known allergy or hypersensitivity to topical photosensitizing agents.
- Subjects with known photosensitivity disorders felt by the investigators to preclude safe inclusion in the study.
Location and Contact Information
Please refer to this study by ClinicalTrials.gov identifier NCT00113425
Michigan
University of Michigan Department of Dermatology, Ann Arbor, Michigan, 48109, United States; Recruiting
Study chairs or principal investigators
John J Voorhees, MD, Study Chair, University of Michigan
More Information
Study ID Numbers: Derm 548
Last Updated: September 12, 2006
Record first received: June 7, 2005
ClinicalTrials.gov Identifier: NCT00113425Health Authority: United States: Institutional Review Board
