Using topical medications to reduce redness from sunlight in rosacea patients
Official title: Pilot Studies Evaluating Use of Topical Imipramine and Amitriptyline in Reducing Ultraviolet B Light-Induced Redness in Patients With Rosacea
Run by Wright State University · NCT06312813 · Data updated 2026-11-12
This study is testing whether two topical medications can help reduce redness from sunlight in people with rosacea.
Quick facts
| Phase | Phase 2 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 48 (estimated) |
| Sponsor | Wright State University Academic / other |
| Drugs / interventions | prednisone |
| Locations | 1 site (Fairborn, Ohio) |
| Status | Recruiting |
| Started | February 27, 2024 |
| Main results expected | December 1, 2028 |
| Study ends | December 1, 2028 |
| Registry record updated | February 18, 2026 |
| Trial ID | NCT06312813 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are individuals with Fitzpatrick Skin Type I to III who have self-identified rosacea or do not have a history of flushing or blushing.
✕Probably not a fit
Patients currently using tricyclic antidepressants or those with recent exposure to certain skin treatments may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical trial evaluates the effectiveness of topical imipramine and amitriptyline in reducing ultraviolet B light-induced redness in patients diagnosed with rosacea. The study aims to determine if these medications can alleviate the skin irritation and redness that often occurs in response to sunlight exposure. Participants will be monitored for their reactions to the treatments, comparing the effects of the active medications against a vehicle control. The trial focuses on individuals with specific skin types and a history of rosacea symptoms.
Why it matters
Potential benefit: If successful, this study could provide a new topical treatment option for patients suffering from rosacea-related redness triggered by sunlight.
How similar studies have gone: While there is limited information on similar studies, the use of topical medications for skin conditions has shown promise in other contexts, suggesting potential for success in this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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. Exclusion Criteria: * 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's running
-
Wright State Physicians
Fairborn, Ohio, United States Recruiting
Study contacts
- Study coordinator: Manager Clinical Research Operations
- Email: pturesearch@wrightstatephysicians.org
- Phone: (937)-245-7500
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.