Registry for patients with lupus at Duke University
Duke Lupus Registry
This study is collecting information and blood samples from people with lupus at Duke University to see how the disease changes over time and improve care for patients.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Duke University Academic / other |
| Locations | 1 site (Durham, North Carolina) |
| Trial ID | NCT00512694 on ClinicalTrials.gov |
What this trial studies
The Duke Lupus Registry collects information and blood samples from patients diagnosed with systemic lupus erythematosus or cutaneous lupus who are seen in the Duke Rheumatology clinics. This observational registry aims to track how lupus changes over time, with the goal of improving patient care and informing future research on various lupus-related outcomes. Patients will complete questionnaires and have their disease activity measured during regular clinic visits, without needing additional appointments. The data collected will help enhance treatment strategies and understand the broader implications of lupus.
Who should consider this trial
Good fit: Ideal candidates are patients diagnosed with systemic lupus erythematosus or cutaneous lupus who are receiving care from a rheumatologist at Duke University Medical Center.
Not a fit: Patients who are unable to travel to Duke for follow-up visits or cannot provide informed consent may not benefit from this registry.
Why it matters
Potential benefit: If successful, this registry could lead to improved treatment strategies and better management of lupus for patients.
How similar studies have performed: Other observational studies on lupus have shown success in improving patient outcomes and understanding the disease, indicating that this approach is supported by prior research.
Eligibility criteria
Show full inclusion / exclusion 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
Where this trial is running
Durham, North Carolina
- Duke University Medical Center — Durham, North Carolina, United States (Recruiting)
Study contacts
- Principal investigator: Megan E. B. Clowse, MD, MPH — Duke University
- Study coordinator: Laura Neil
- Email: laura.k.neil@duke.edu
- Phone: (919) 684-8936
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.