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Recruiting NCT06921239

HLA Antibodies in Systemic Lupus Erythematosus

Observational HLA Antibodies Systemic Lupus Erythematosus

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: HLA Antibodies, Systemic Lupus Erythematosus. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Patients suffering from autoimmune diseases show false-positive results when anti-HLA antibodies are identified. This false positivity makes it difficult to obtain an organ transplant based on immunological compatibility (absence of anti-HLA antibodies directed against graft antigens). The objectives of this project are to study the prevalence of these false positivities in a population of lupus patients, and to evaluate biological tests that can negate these false positivities.

Primary outcome measures

  • prevalence of unexplained antibody positivity [Time frame: 6 months]

Eligibility criteria

Inclusion criteria

  • Patients Adults
  • Followed in the internal medicine department of Amiens University Hospital - With systemic lupus erythematosus
  • Without HLA immunization risk factors (no history of pregnancy, transfusions or transplants)
  • With sera stored in the biobank

Exclusion criteria

  • minor Patients
  • Opposing the re-use of their personal data for research purposes

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

France · 1 center
  • CHRU Amiens — Amiens

Identifiers

NCT: NCT06921239 · PI2025_843_0043

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗