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RECRUITING
NCT04520217
PHASE1

Testing Use of Topical Imipramine in Reducing Ultraviolet B Induced Microvesicle Particle Release in Photosensitive Subjects

Sponsor: Wright State University

View on ClinicalTrials.gov

Summary

The purpose of this study is three-fold. First, researchers will assess whether subjects who have clinically abnormal reactions to sunlight (photosensitivity) have increased levels of microvesicle particles (MVP) following ultraviolet B (UVB) treatment to localized area of skin. Second, researchers will assess if topical application of the medicine imipramine will block UVB-induced MVP release. Third, researchers will assess if the topical cream will block UVB-induced increased erythema reactions (reddening of the skin).

Official title: Pilot Studies Testing Use of Topical Imipramine in Reducing Ultraviolet B Induced Microvesicle Particle Release in Photosensitive Subjects

Key Details

Gender

All

Age Range

18 Years - 50 Years

Study Type

INTERVENTIONAL

Enrollment

40

Start Date

2022-06-06

Completion Date

2026-12-01

Last Updated

2025-01-27

Healthy Volunteers

Yes

Interventions

DRUG

4% Imipramine Cream

4% Imipramine Cream

DRUG

Base Cream

Base Cream

Locations (1)

Wright State Physicians

Fairborn, Ohio, United States