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Study identifier: NCT06820866 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Non-invasive Diagnosis of Idiopathic Nephrotic Syndromes

Condition: Idiopathic Nephrotic Syndrome (INS)  ·  Sponsor: Assistance Publique - Hôpitaux de Paris

PhaseN/A
Planned participants265
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Renal biopsy (RB) is the reference diagnostic procedure for Idiopathic Nephrotic Syndrome (INS). It is an invasive procedure, particularly risky during the acute phase of nephrotic syndrome when anticoagulation therapy is required. By identifying serum antibodies that allow for the non-invasive diagnosis of the main differential diagnoses of INS, (Membranous Nephropathy), the development of a non-invasive diagnostic tool for INS could help reduce the morbidity associated with the invasive renal biopsy procedure, minimizing the risk of incorrect diagnosis. We developed a diagnostic score, the SNIT, from routine clinical and biological variables to allow INS diagnoses in patients for whom detection of blood antibodies of Membranous Nephropathy were negative. The main goal of this study is to validate this diagnosis score in a prospective study, to allow INS diagnosis without renal biopsy.

This description comes directly from the study's public registry record.

Talk to the study team

Alexandre LAHENS, Dr  ·  +33 1 56 01 70 43  ·  alexandre.lahens@aphp.fr

Jean-Jacques BOFFA, Pr  ·  +33 1 56 01 60 29  ·  jean-jacques.boffa@aphp.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Service de Néphrologie et Dialyses, Hôpital TenonParis, France, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT06820866