Duke Lupus Registry

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?

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