Systemic Lupus Registry
The Systemic Lupus International Collaborating Clinica (SLICC) Registry for Atherosclerosis in SLE
Protocol ID
07-053
Protocol Description
The purpose of this study is to establish an international registry of lupus patients. The registry will collect information and blood samples on a yearly basis, on a large number of patients newly diagnosed with systemic lupus erythematosus (SLE).
This registry will provide for the long-term follow-up of a large diverse population of patients and may allow researchers to determine some of the risk factors for heart disease in patients with SLE.
Eligibility Criteria
Patients with systemic lupus erythematosus (SLE)
Primary Investigator(s)
- Cynthia Aranow, MD