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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00512694
Other study ID # Pro00008875
Secondary ID 8652-07-6R1
Status Recruiting
Phase
First received
Last updated
Start date July 2007
Est. completion date June 2027

Study information

Verified date December 2023
Source Duke University
Contact Laura Neil
Phone (919) 684-8936
Email laura.k.neil@duke.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Lupus is a systemic autoimmune disease that can present with many varied symptoms, including joint pain, fevers, kidney disease, and rashes. Lupus can affect anyone, but it is most common in younger women. The Duke Lupus Registry will collect information and blood samples from patients with lupus (systemic lupus erythematosus or cutaneous lupus) seen in the Duke Rheumatology clinics. The goal of this Registry is to understand how lupus changes over time so that we can improve the treatment of patients with lupus.


Description:

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date June 2027
Est. primary completion date June 2027
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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


Locations

Country Name City State
United States Duke University Medical Center Durham North Carolina

Sponsors (1)

Lead Sponsor Collaborator
Duke University

Country where clinical trial is conducted

United States, 

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