Evaluating Use of Topical Imipramine and Amitriptyline in Reducing Ultraviolet B Light-Induced Redness in Patients With Rosacea
Recruiting now · Phase 2
Conditions studied: Rosacea
In brief
Rosacea is a common skin condition associated with easy blushing and red face; many patients with rosacea react to sunlight with increased redness. The purpose of this study is to determine if the use of a topical medication will help reduce sunlight induced redness and irritation in patients with rosacea.
Key facts
- Study ID
- NCT06312813
- Run by
- Wright State University
- People needed
- 48
- Starts
- 2024-02-27
- Expected to finish
- 2028-12-01
- Last updated by the study team
- 2026-02-18
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Fitzpatrick Skin Type I - IIII
- Self-identified rosacea or no history of flushing/blushing for controls
- Able to provide medical history and list of medications -- control subjects will not be allowed to take medications that are known to be photosensitizers.
You may not qualify if…
- Using imipramine, amitriptyline or any other tricyclic antidepressant (oral or topical)
- Using topical anti-inflammatory (within 1 week) or systemic agents (e.g. prednisone)
- Large tattoos in the designated testing areas
- Tanning bed use within last 3 months
- Photodynamic Therapy or UCB treatments in past 3 months
- Female Subjects: pregnant or nursing
Where it is running
- Wright State Physicians — Fairborn, Ohio, United States (enrolling)
Full record on ClinicalTrials.gov
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