Clinical Responsiveness of Dermatomyositis Using Cutaneous Dermatomyositis Disease Area and Severity Index (CDASI)

Recruiting Observational Study
Dermatomyositis
No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
300 (estimated)
Sponsor
University of Pennsylvania · Other
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About This Trial
The Evaluation of Clinical Responsiveness Using the Cutaneous Dermatomyositis Disease Area and Severity Index (CDASI), established in 2008, is a one-site database study conducted at the University of Pennsylvania. The database has yielded valuable information and clinical insights into the pathophysiology, disease processes, including psychological responses, treatments and quality of life associa…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Gender/Age: Males or females above 18 years old * Diagnosis: Cutaneous Dermatomyositis * Subjects able to give informed consent Exclusion Criteria: * Subjects without cutaneous DM * Penn employees * Penn students * Cognitively impaired persons
Contacts

Victoria Werth, MD

215-615-2940

werth@pennmedicine.upenn.edu

CONTACT

Joyce Okawa, RN

215-615-2940

joyce.okawa@pennmedicine.upenn.edu

CONTACT