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Clinical implementation of an uveitis prediction model

Clinical implementation of an uveitis prediction model - Uveitis prediction model

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON46803
Enrollment
250
Registered
2018-05-16
Start date
2019-04-04
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

Uveitis

Interventions

Sponsors

Oogziekenhuis Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Non-infectious uveitis. - Age >= 18 years. - Informed consent.

Exclusion criteria

Exclusion criteria: - Major eye condition preventing any VA improvement or reduction (such as end stage glaucoma, end stage corneal diseases, end stage macular degeneration). - Suspected or proven infectious uveitis. - Masquerade syndromes (such as intraocular B cell lymphoma). - Patients for whom all data of the first year since onset of their uveitis are missing. - Patients for whom, since onset of their uveitis, data (> 3 years) are missing.

Design outcomes

Primary

MeasureTime frame
Best corrected visual acuity.

Secondary

MeasureTime frame
Duration and dose immunosuppressives. See Ch. 8 of the protocol.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)