RecruitingRecruiting
Duke Lupus Registry
NCT00512694 · Duke University
In plain English
Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.
About this study
The Duke Lupus Registry is a prospective cohort comprised of patients with lupus seen in the Duke Rheumatology clinic.
The Duke Lupus Registry has two main purposes:
1. Improved patient care. By following disease activity scores and medication usage, we expect to improve our care of the patients seen in clinic.
2. Future research on lupus outcomes. This may encompass a broad array of areas, including but not limited to cardiovascular health, pregnancy and fertility, infections, medication use, quality of life, and depression.
At each office visit, patients will complete a questionnaire, physicians will measure lupus activity, and patients may be asked to provide a small blood sample. Patients will not be required to make extra visits to Duke in order to participate -- all paperwork and blood draws will occur during a regularly scheduled office visit with the physician.
Eligibility criteria
Inclusion Criteria:
* Diagnosis of Systemic Lupus Erythematosus or Cutaneous Lupus
* Patient of a rheumatologist at Duke University Medical Center
Exclusion Criteria:
* Inability to travel to Duke for follow-up visits
* Inability to speak English
* Not able to provide informed consent
Study design
Enrollment target: 1000 participants
Age groups: adult, older_adult
Timeline
Starts: 2007-07
Estimated completion: 2028-06
Last updated: 2026-01-08
Sponsor
Duke University · other
Contacts & investigators
ContactLaura Neil · contact · laura.k.neil@duke.edu · (919) 684-8936
InvestigatorMegan E. B. Clowse, MD, MPH · principal_investigator, Duke University
All locations (1)
Duke University Medical CenterRecruiting
Durham, North Carolina, United States