Combination Gel and Vascular ND in Mild to Moderate Rosacea

Wake Forest University Health Sciences10 enrolled

Overview

This is a single center, open-label, split-face, prospective study of ten to fifteen subjects seeking vascular laser therapy for the treatment of mild to moderate rosacea. Subjects will be screened for eligibility for vascular laser therapy outside of the confines of this protocol. Once approved for laser, subjects will be screened for study enrollment and topical treatment of their rosacea at the Screening/Baseline visit. All subjects will receive Finacea 15% gel and will be instructed to apply the study drug to one half of the face, twice daily. Drug application will be modified just prior to and after the subjects' laser treatment to reduce irritation. Subjects will undergo Vascular Nd:Yag laser therapy to involved areas over the whole face two weeks after initiating Finacea treatment. Subjects will continue to use Finacea gel to one half of the face for the duration of the study.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Male or female subject with mild to moderate rosacea, age 18 and over, who agrees to participate and provide written consent. * Have an Investigator Global Assessment of mild to moderate rosacea (IGA rating between 2 and 5 in the Investigator Global Assessment (Appendix B) and at least a "Mild" rating on the Telangiectasia Rating Scale * Subjects must be eligible to undergo vascular laser therapy and have been previously approved for therapy. Exclusion Criteria: * Initiation or change in dose within 4 weeks of baseline of systemic anti-inflammatory medication which may influence study outcome. * Use of topical therapy for rosacea within 2 weeks of baseline. * Use of systemic corticosteroids within 4 weeks of baseline. * Use of systemic retinoids within 6 months of baseline * Presence of a concurrent medical condition or skin condition, which is determined by the investigator to potentially interfere with study outcomes or patient assessments. * Amount of disease involvement that would require \>60 gm of cream in a 6 week period. * Subjects with known allergy or sensitivity to azelaic acid (Finacea®) gel or components therein, such as propylene glycol. * Contraindication to vascular laser therapy, such as infections. * Female subjects who are not postmenopausal for at least 1 year, surgically sterile, or willing to practice effective contraception during the study. Reliable methods of birth control are: abstinence (not having sex), oral contraceptives, intrauterine device (IUD), DepoProvera, tubal ligation, or vasectomy of the partner (with confirmed negative sperm counts) in a monogamous relationship (same partner). An acceptable, although less reliable, method involves the careful use of condoms and spermicidal foam or gel and/or a cervical cap or sponge. Nursing mothers, pregnant women and women planning to become pregnant while on study are to be excluded.

Outcomes

Primary Outcomes

IGA of Improvement

Investigator's Global Assessment of severity integrates all lesions for overall score. This measure is commonly used as a quick and simple way to quantify disease severity both for clinical studies and in a non-study clinic setting. Score ranges from 0 = Clear or "No inflammatory signs of rosacea" to 6 = "Severe inflammatory signs of rosacea."

Time frame: 6 weeks

Combination Gel and Vascular ND in Mild to Moderate Rosacea

Overview

Conditions

Interventions

Eligibility

Locations (1)

Outcomes

Primary Outcomes