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.
Who Can Participate?
Eligibility
Adults diagnosed with lupus
Age Range
18-110
Sex/Genders
Male (cisgender)
Female (cisgender)
Non-binary or gender fluid
Transgender male
Transgender female
Looking for Healthy Participants
No
What is Involved?
Description
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.
Locations
Duke University Hospital
Compensation
No
Spanish Materials Available
No
Study Details
Full Title
Duke Lupus Registry
Principal Investigator
Jennifer
Rogers
Protocol Number
PRO00008875
NCT ID
NCT00512694
Enrollment Status
Open to Enrollment