Registry of Argentinian patients with lupus

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This project aims to create a longitudinal cohort of Argentinian patients diagnosed with systemic lupus erythematosus (SLE) to gather real-world data over a five-year follow-up period. The study will collect data from patients' clinical histories, focusing on sociodemographic information, clinical manifestations, treatment access, and patient-reported outcomes. Experienced physicians will oversee data collection using a specially designed electronic case report form to ensure accuracy and facilitate research inquiries.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patients ≥ 18 years of age
* Classified as SLE (according to the 1982/1997 American College of Rheumatology criteria and/or Systemic Lupus International Collaborating Clinics criteria for SLE)
* Less than 5 years from meeting SLE criteria
* Informed consent signature

Exclusion Criteria:

* Diagnosis of other systemic autoimmune diseases or overlap syndromes
* Patients who have been transferred to other centers

Where it's running

• Lucila Garcia
  La Plata, Buenos Aires, Argentina Recruiting

Study contacts

• Study coordinator: Guillermo Pons-Estel, PhD
• Email: unisar@reumatologia.org.ar
• Phone: +543414498750

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.