Open Actively Recruiting

Lupus Landmark Study: A Prospective Registry and Biorepository

About

Brief Summary

The purpose of the registry and biorepository is to provide a mechanism to store clinical data, linked biospecimens and molecular data to support the conduct of future research on Systemic Lupus Erythematosus (SLE), including Lupus Nephritis (LN).

Study Type
The nature of the investigation or investigational use for which clinical study information is being submitted. Learn more
Observational

Eligibility

Gender
All
Healthy Volunteers
No
Minimum Age
18 Years
Maximum Age
110 Years

Inclusion Criteria:

  • Able to understand and comply with study procedures and voluntarily sign a written informed consent document
  • Age 18 years or older at the time of enrollment
  • Fulfill criteria for SLE based on one or more of the following classifications systems: Systemic Lupus Erythematosus International Collaborating Clinic (SLICC) 2012 criteria; European Alliance of Associations for Rheumatology (EULAR)/American College of Rheumatology (ACR) 2019 criteria; 1997 revised ACR criteria; or Lupus is present per clinical assessment.

Exclusion Criteria:

  • Not able to obtain consent
  • Not able to meet protocol visit requirements
  • Pregnant at the time of enrollment
Study Stats
Protocol No.
24-5136
Category
Autoimmune Disorders
Principal Investigator
Maureen A. McMahon, MD
Maureen A. McMahon, MD
Rheumatology
Maureen A. McMahon, MD
Contact
  • Grace Harvey
Location
  • UCLA Westwood
For Providers
NCT No.
NCT05934149
For detailed technical eligibility, visit ClinicalTrials.gov.