Skip to content

An observational neuroimaging and neurophysiological study investigating the visual pathway in Huntington*s disease.

An observational neuroimaging and neurophysiological study investigating the visual pathway in Huntington*s disease. - Visual pathway in HD.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON45518
Enrollment
60
Registered
2017-04-12
Start date
2017-01-16
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

hereditary neurodegenerative movement disorder Huntington's disease

Interventions

Huntington's disease
Visual cortex
Visual-Evoked Potentials

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: * Between 18 and 65 years of age at time of visit * Ability to undergo MRI scanning * Written informed consent must be obtained from the participant;If the participant is a manifest HD gene carrier: * Gene positive tested with CAG repeat length of * 36 in the HTT gene * UHDRS-TMS > 5;If the participant is a premanifest HD gene carrier: * Gene positive tested with CAG repeat length of * 36 in the HTT gene * UHDRS-TMS * 5;If the participant is a control subject: * Gene negative tested for HD or without family history of HD * No other known cognitive, neurological or psychiatric disorders

Exclusion criteria

Exclusion criteria: * Impaired primary visual ability (

Design outcomes

Primary

MeasureTime frame
* Group differences and correlations between pre- and manifest HD and healthy controls on the functional and structural MRI outcome parameters. * Correlation between scores on neuropsychological assessments and MRI outcome parameters in all groups. * Differences in VEP outcome measures (amplitudes and latencies) between pre-, manifest HD and healthy controls. * Correlation between VEP outcome measures and outcome parameters of different imaging modalities (e.g. fMRI, DTI and structural MRI).

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)