Elucidating the genetic pathomechanism underlying rare and hereditary kidney diseases

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00008910

Enrollment

3000

Registered

2016-06-16

Start date

2015-11-18

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

N18

Interventions

Group 1: Genetic examination of patients suffering from hereditary, unclear and rare kidney diseases accompanied by a molecular analysis of urine, stool and blood

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Suspected rare or inherited kidney disease

Exclusion criteria

Exclusion criteria: none

Design outcomes

Primary

Measure	Time frame
genetic diagnosis of rare and unclear kidney diseases	—

Secondary

Measure	Time frame
Analyis of the pathophysiological processes caused by the genetic change	—

Countries

Germany

Contacts

Public ContactCornelia Böhme

Klinik II für Innere MedizinUniklinik Köln

cornelia.boehme@uk-koeln.de0221-478-97222

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026