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Network for Early Onset Cystic Kidney Diseases

Network for Early Onset Cystic Kidney Diseases - NEOCYST

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00011003
Enrollment
500
Registered
2016-09-06
Start date
2016-08-18
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Q61.1 Q61.3 Q61.8 Q61.9 Q87.5 Q87.8 Q77.2 Q77.6 Q77.9

Interventions

Group 1: The clinical data of all patients with the above mentioned diseases will be documented and followed-up once a year. Additionally they can provide biological samples and participate in diverse

Sponsors

Universitätsklinikum Münster, Klinik für Kinder-und Jugendmedizin, Allgemeine Pädiatrie, Leiter Pädiatrische Nephrologie, Stellvertretender Direktor Allgemeine Pädiatrie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: all patients with the above ICD-10 codes

Exclusion criteria

Exclusion criteria: all patients presenting other diseases than the ones presented above

Design outcomes

Primary

MeasureTime frame
The primary objective of the multidisciplinary network NEOCYST is to improve the life of patients and their families affected by hereditary cystic kidney diseases by increasing our knowledge of the epidemiology, genetics, molecular pathophysiology and long-term outcomes of pediatric cystic kidney disease with and without extrarenal manifestations.

Countries

Austria, Germany, Switzerland

Contacts

Public ContactJens König

Universitätsklinikum Münster, Pädiatrische Nephrologie

jens.koenig@ukmuenster.de0251 / 83-56215

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: May 1, 2026