# Set-up of a Platform for Personalized Diagnosis of Rare Kidney Diseases (NIKE)

> **NCT06325072** · NA · UNKNOWN · sponsor: **Meyer Children's Hospital IRCCS** · enrollment: 160 (estimated)

## Conditions studied

- Chronic Kidney Diseases

## Interventions

- **DIAGNOSTIC_TEST:** Conclusive genetic testing
- **DIAGNOSTIC_TEST:** Genotype-phenotype correlation for personalized diagnosis
- **DIAGNOSTIC_TEST:** Personalized study of variants of uncertain clinical significance (VUS) through functional studies on 3D organ-on-a-chip

## Key facts

- **NCT ID:** NCT06325072
- **Lead sponsor:** Meyer Children's Hospital IRCCS
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2021-07-09
- **Primary completion:** 2023-06-27
- **Final completion:** 2024-06-30
- **Target enrollment:** 160 (ESTIMATED)
- **Last updated:** 2024-03-22


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06325072

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06325072, "Set-up of a Platform for Personalized Diagnosis of Rare Kidney Diseases (NIKE)". Retrieved via AI Analytics 2026-05-27 from https://api.ai-analytics.org/clinical/NCT06325072. Licensed CC0.

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