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Genetics of childhood glaucoma in the Netherlands

Genetics of childhood glaucoma in the Netherlands - Genetics of childhood glaucoma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON56998
Enrollment
437
Registered
2024-09-11
Start date
2024-10-21
Completion date
Unknown
Last updated
2025-08-25

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

Conditions

childhood glaucoma glaucoma in children

Interventions

None listed

Sponsors

Amsterdam UMC
Lead Sponsor

Eligibility

Age
No minimum to 99 Years

Inclusion criteria

Inclusion criteria: Patients with childhood glaucoma - without a glaucoma gene panel screening; or - with a negative glaucoma gene panel

Exclusion criteria

Exclusion criteria: patients with childhood glaucoma where a gene mutation have been found

Design outcomes

Primary

MeasureTime frame
Primary outcomes are a mutation in one of the 26 known glaucoma genes of the gene panel, a new gene mutations found with whole exome sequencing (WES), or no gene mutation.

Secondary

MeasureTime frame
Secondary study parameters are the genotype-phenotype study where we link the clinical findings to the gene mutation

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)