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Genetic identification and genotype-phenotype study in inherited cystic kidney disease

Genetic identification of hereditary cystic kidney diseases for implementing precision medicine

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0005580
Enrollment
1200
Registered
2020-11-05
Start date
2019-10-07
Completion date
Unknown
Last updated
2020-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Seoul National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with 3 or more cysts in kidneys - Typical ADPKD - Atypical ADPKD - Tuberous sclerosis complex - von Hippel-Lindau disease - Autosomal dominant tubulo-interstitial kidney disease - Autosomal recessive polycystic kidney disease - Nephronophthisis

Exclusion criteria

Exclusion criteria: Those who are not able to give informed consent or pregnant will be excluded from enrollment. The cases of simple renal cyst and acquired cystic kidney disease which involve cyst formation as the result of renal failure will also be excluded from this study.

Design outcomes

Primary

MeasureTime frame
Novel cystogenesis-related genes—

Secondary

MeasureTime frame
Genes related to the severity of disease—

Countries

Korea, Republic of

Contacts

Public ContactHayne Park

Hallym University Medical Center-Kangnam

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 24, 2026