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Ophthalmic Imaging in HCHWA-D

Ophthalmic Imaging in HCHWA-D - Ophthalmic Imaging in HCHWA-D

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON40430
Enrollment
60
Registered
2014-10-22
Start date
2014-10-01
Completion date
Unknown
Last updated
2024-04-23

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

Conditions

Hereditary Cerebral Hemorrhage With Amyloidosis-Dutchtype

Interventions

None listed

Sponsors

Oogheelkunde
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: DNA-proven patients with HCHWA-D or patients with a strong clinical suspicion for HCHWA-D in combination with MRI-scan abnormalities highly suggesting HCHWA-D. Patients must be willing to be informed about their test results and (clinical) diagnosis.

Exclusion criteria

Exclusion criteria: Direct family members of the patients whom genetic testing is not performed and/or are nog willing to be informed about their test results and (clinical) diagnosis; Age-related Macular Dystrophy (AMD); Diabetic Mellitus; Macular dystrophies; Eye traumas; Glaucoma

Design outcomes

Primary

MeasureTime frame
Differences between the opthalmic findings in HCHWA-D patients and controls.

Secondary

MeasureTime frame
-

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)