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NCT07763834Not yet recruiting

Uromodulin as a Biomarker in Lupus Nephritis

Evaluation of Uromodulin as a Biomarker of Renal Histological Activity/ Chronicity Indices in Lupus Nephritis

Source: ClinicalTrials.gov · Last updated 13 Aug 2026

Brief summary (registry, in English)

Evaluation of Uromodulin as a biomarker of renal histological activity/ Chronicity indices in lupus nephritis

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
90 (estimated)
First submitted
9 Aug 2026
Start date
1 Oct 2026
Primary completion date
2 Aug 2029
Lead sponsor
Assiut University
Diseases
Lupus (SLE)
NCT number
NCT07763834

What you commit to

  • Study type: Observational
  • Planned participants: 90
  • From 1 Oct 2026 to the primary completion date, 2 Aug 2029
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Who the study is looking for

  • • Group I: 30 patients with different classes of Lupus Nephritis. These cases are biopsy proven
    • LN. Histological diagnosis of LN is according to the revised International Society of
    • Nephrology/ Renal Pathology Society (ISN/RPS) classification and modified National Institute of Health (NIH) activity and chronicity indices (Bajema et al 2018) .
  • Biopsy-proven lupus nephritis at the time of uromodulin blood sampling.
  • Group II: 10 patients with active SLE without renal involvement and with SLEDAI score ≥6
  • Group III: 10 patients with non-active SLE with SLEDAI score \<6
  • Group IV: 30 patients with primary forms of non-lupus Glomerulonephritis
  • Group V: 10 healthy control subjects
  • All cases are adults ≥18 years.
  • Diagnosis of systemic lupus erythematosus according to the 2019 EULAR/ACR Classification
    • Criteria (Ref).Exclusion Criteria:
  • • .Pregnancy or lactation
    • AKI secondary to pre renal OR post renal cause (from clinical history and imaging).
    • End-stage renal disease requiring dialysis
    • Active infection or sepsis
    • Active malignancy (either under treatment or within 5 years of successful treatment)
    • History of renal transplantation
    • Heart failure with NYHA III and IV
    • Hhistory of other autoimmune diseases or diabetes mellitus

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.