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Recruiting Not applicable

Immunopathological Analysis in a French National Cohort of Membranous Nephropathy

NCT04326218 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2020-07-04
Last updated
2026-06-16

Condition(s) studied

Membranous Nephropathy

Investigational drug(s) / intervention(s)

Blood sample

Blood sample: Serum samples will be sent for centralised analyses in Nice. On these samples, different analysis will be performed : * anti-PLA2R1 and anti-THSD7A antibodies * anti-PLA2R1 and anti-THSD7A epitopes * HLA typing

Study summary

National cohort of all cases of membranous nephropathy (MN) during a 1 year period in France, based on a pathological and/or serological diagnostic, collecting the data on:

* incidence of MN
* prevalence of anti-PLA2R1 and anti-THSD7A
* clinical outcome one year after diagnosis or after relapse (complete remission, partial remission or persistent nephrotic syndrome)
* environmental risk factors for the onset of MN
* HLA markers
* patient care status in France

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age 18 years or more * Biopsy on a native kidney consistent with MN and/or positivity for serum anti-PLA2R1 and/or anti-THSD7A antibodies * Signed informed consent Exclusion Criteria: * Diagnosis error based on the kidney biopsy staining or on serology analyses for the positivity for anti-PLA2R1 and/or anti-THSD7A * Patients unable to give an informed consent * Patients withdrawing an informed consent

Primary outcome measure(s)

  • To determine the incidence of Membranous Nephropathy (MN) and its evolution — one year after inclusion
    as either complete remission (UPCR \< 0.3 g/g, serum albumin \> 35 g/L, eGFR \> 60 ml/min/1.73 m²) or partial remission (UPCR \< 3.5 g/g and reduction of at least 50% from baseline, \< 20% increase of serum creatinin from baseline) or persistent nephrotic syndrome (UPCR \> 3.5 g/g, serum albumin \< 30 g/L)

Trial sites (1)

FacilityCityRegionStatus
CHU de Nice, Hôpital de l'Archet Nice Alpes Maritime Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04326218 on ClinicalTrials.gov ↗ ← All trials in France