Duke Lupus Registry - Clinical Trial
What is the Purpose of this Study?
A registry is a database of information (data) about patients living with a specific condition. Scientists study the information in the registry to increase what we know about the condition so we can develop better treatments in the future.
This registry will help us better understand lupus and how it is managed, including how different treatments work and their long-term safety.
Systemic Lupus Erythematosus (Lupus, or SLE)
Who Can Participate in the Study?
Adults diagnosed with lupus
What is Involved?
If you choose to join the registry, we will collect and store your blood and/or urine samples along with your medical information for current and future studies.