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A National Prospective Cohort of Patients With Idiopathic Nephrotic Syndrome Beginning in

Pediatric idiopathic nephrotic syndrome (INS) is a rare disease for which the optimal therapeutic strategy has not yet been defined. A network of clinicians treating complicated forms of this disease (grouped within the Société de Néphrologie Pédiatrique, SNP) exists, but to date there is no prospective cohort followin

Condition(s)Idiopathic Nephrotic Syndrome
StatusRecruiting
Study typeObservational
SummaryPediatric idiopathic nephrotic syndrome (INS) is a rare disease for which the optimal therapeutic strategy has not yet been defined. A network of clinicians treating complicated forms of this disease (grouped within the Société de Néphrologie Pédiatrique, SNP) exists, but to date there is no prospective cohort following up these patients that would facilitate the development of cohort-nested trials. This absence of structured follow up makes it difficult to set up prospective studies. The main objective is to create a prospective cohort of pediatric INS patients to collect cases treated in SNP centers, to study their epidemiological characteristics, and to provide a basis for comparison for future cohort-nested trials.
Who can participateInclusion Criteria: * Patient under 18 years of age * With idiopathic nephrotic syndrome (according to SPN criteria) beginning after January 1, 2018 * Child seen at least once in consultation or hospitalization by a pediatrician member of the Society of Pediatric Nephrology * Residing in France * Consent signed by parents and patient's agreement to participate (if of age) * Affiliated to a social security system. Exclusion Criteria: * Refusal of the patient or legal representatives to participate in the cohort
Ages18 Years
SexAll
Lead sponsorUniversity Hospital, Limoges
LocationsAgen, France; Amiens, France; Auxerre, France; Bayonne, France; Besançon, France; Bordeaux, France (+42 more sites)
Start date2020-03-13
NCT IDNCT04207580
Official listinghttps://clinicaltrials.gov/study/NCT04207580

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