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An Analysis of the Effect of Topical Cromolyn Sodium on Rosacea-associated Erythema

Papulopustular Rosacea Clinical Trial

Official title:
An Analysis of the Effect of Topical Cromolyn Sodium on Rosacea-associated Erythema

Clinical Trial Summary

This study is designed to investigate whether topical application of a cromolyn sodium solution is able to decrease the facial redness seen in patients with papulopustular rosacea. Previous work in the lab of Dr. Di Nardo on mice has suggested that cromolyn may be able to have this effect. The study will enroll a total of 10 patients. 5 will randomly be assigned to receive the cromolyn sodium solution, and the other 5 will be randomly assigned to receive the placebo solution. All participants will be instructed to apply their assigned solution twice daily to their face. Patients will return to the clinic 3, 6, and 8 weeks after the distribution of the solutions to measure the efficacy of their assigned solution.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01933464
Study type Interventional
Source University of California, San Diego
Contact
Status Completed
Phase Phase 1/Phase 2
Start date August 2013
Completion date April 2014
View Details
See also
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