An Observational Study to Assess Patient Satisfaction & Control of

Clinical Trial Summary

The purpose of this study is to document quality of life, patient satisfaction, effect on itching, and control of psoriasis vulgaris associated with use of calcipotriene/betamethasone dipropionate (Taclonex®) topical suspension 0.005% / 0.064% for treatment of plaque psoriasis under real-life conditions.

See also
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NCT number	NCT01982552
Study type	Observational
Source	LEO Pharma
Contact
Status	Completed
Phase	N/A
Start date	July 2013
Completion date	January 2014

An Observational Study to Assess Patient Satisfaction and Control of Psoriasis With Calcipotriene/Betamethasone Dipropionate (Taclonex®) Topical Suspension, and Effect on Quality of Life

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms