Clinical Trial

Brimonidine 0.33% for Rosacea-Related Facial Erythema

Completed Phase 4
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Summary
This study looks at whether a topical gel called 0.33% brimonidine can reduce persistent facial redness caused by rosacea. The study was carried out in two parts. In the first part, the gel was applied to only one side of each participant's face, while the other side received a placebo (a non-active gel). Redness was measured before and after application to see the immediate (short-term) effect. In the second part, participants used brimonidine gel on both sides of the face once daily for one month. Redness and visible blood vessel changes were checked again at the end of this period. Redness was evaluated using objective measurements of skin color, dermoscopic (magnified) images of facial blood vessels, and patient-reported symptoms such as burning or stinging. The purpose of this study is to understand both the short-term and one-month effects of 0.33% brimonidine gel on persistent facial redness in people with rosacea.
Trial Details
NCT Number NCT07431476
Lead Sponsor Istanbul Training and Research Hospital
Conditions Rosacea, Rosacea Subtype 1 (Erythematotelangiectatic)
Enrollment 45 participants
Start Date 2025-05-01
Primary Completion 2025-08-07 (estimated)
Study Completion 2025-08-07 (estimated)
Updated on ClinicalTrials.gov 2026-02-24