HairMax LaserComb Open Label Study to Treat Seborrheic Dermatitis

Lexington International

Status

Completed

Conditions

Seborrheic Dermatitis

Treatments

Device: HairMax LaserComb

Study type

Interventional

Funder types

Industry

Identifiers

NCT00830908

LEX0903

Details and patient eligibility

About

The purpose of this study is to test whether the stimulation of vascularization and cellular metabolism on the scalp by use of the HairMax LaserComb will produce improvement in the condition of scalp seborrheic dermatitis.

Full description

This is an open label pilot study to evaluate the effects of the low-level laser light on seborrheic dermatitis of the scalp. Dandruff assessment scores for scalps with seborrheic dermatitis will be assessed at baseline with monthly evaluations during treatment, until final assessment at end of treatment at week 12.

The trial will involve 10 patients aged 18 years and older with a diagnosis of seborrheic dermatitis. Patients will use the LaserComb device three times per week on non-consecutive days for 12 weeks. No other seborrheic dermatitis products will be used during treatment. The investigator will conduct measurements of dandruff at each study visit, as a measure of efficacy.

The trial consists of 4-5 study visits (screening/baseline, week 4, week 8 and week 12). Dandruff evaluation and adverse event assessments will be performed at each visit.

Safety analysis will be assessed based on the reports of adverse events during the study.

Enrollment

10 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Diagnosis of seborrheic dermatitis of the scalp
PGA of 2 (mild) or greater at baseline
TDSS score at baseline of 2 or greater, for both scaling and inflammation
Must agree to use of non-medicated shampoos during study period; must refrain from use of other medicated scalp products during the trial

Exclusion criteria

Use of any topical or oral products that would affect assessment of the scalp SD condition, in the opinion of the primary investigator, within the following periods prior to baseline:
- Medicated shampoos within 2 weeks of baseline
- Topical scalp medications within 2 weeks of baseline
- Oral medications affecting the scalp within 4 weeks of baseline
- Other medications determined by the investigator to potentially affect the assessment of SD = washout to be determined by the investigator, as appropriate to the known medication properties
Any current or past medical condition, including active dermatitis or any other dermatological condition, which might interfere with assessment of dandruff
Patients using any medications that may increase photosensitivity, and thus pose a risk when undergoing LaserComb therapy
Patients with known adverse reactions, allergy or hypersensitivity to laser light components/light sensitivity conditions
Patients who have received any investigational drug within 30 days prior to study entry.