drugset / Trial / NCT07431476

Brimonidine 0.33% for Rosacea-Related Facial Erythema

NCT07431476

Phase 4 Completed 45 enrolled Istanbul Training and Research Hospital
RandomizedParallel-groupDouble-blindTreatment

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.

Timeline

Start
2025-05-01
Primary completion
2025-08-07
Completion
2025-08-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Brimonidine Small molecule 0.33 % Topical

Indications