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Clinical Trial Summary

To compare the effectiveness, safety (tolerability), and duration of treatment response at 12 weeks of home versus office-based narrowband ultraviolet B phototherapy for the treatment of psoriasis


Clinical Trial Description

The primary objective of this study is to compare the effectiveness, safety (tolerability), and duration of treatment response at 12 weeks of home versus office-based narrowband ultraviolet B phototherapy for the treatment of psoriasis. Physician Global Assessment (PGA) and Dermatology Life Quality Index (DLQI) will be used to assess effectiveness, safety (tolerability), and duration of treatment response. This is a three year pragmatic, randomized, active comparator effectiveness study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03726489
Study type Interventional
Source University of Pennsylvania
Contact
Status Completed
Phase N/A
Start date March 1, 2019
Completion date December 30, 2023

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