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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02407886
Other study ID # 2014-0649
Secondary ID
Status Completed
Phase N/A
First received March 5, 2015
Last updated May 24, 2017
Start date March 2015
Est. completion date May 2016

Study information

Verified date May 2017
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Transsynaptic degeneration of the retinogeniculate pathways is well documented to occur in nonhuman primates when the cerebral lesion occurs even during adulthood. In case of humans, retrograde transsynaptic degeneration of the retinogeniculate pathways has been shown to occur following prenatal or perinatal lesions, but its occurrence after cerebral lesions in adults is considerable rare. It is, however, well established that retrograde transsynaptic degeneration affects other neural systems in humans even when the injury occurs during adulthood. Some histopathological evidence points to the possibility of transsynaptic degeneration of the retinogeniculate pathway in humans even when the lesion occurs in adults, but the clinical significance is unknown.'

Purpose:

To measure the retinal ganglion cell layer (GCL) in patients with visual field defects due to intracerebral processes. To correlate GCL with the localization and type of intracerebral lesion.

To compare the GCL with the retinal nerve fibre layer (RNFL) to investigate, which of the 2 parameters is more sensitive to show retinal layer abnormalities.

To correlate GCL with visual field defects and electrophysiological parameters.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date May 2016
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- adult patients with intracerebral lesions within the central visual tract

- associated visual field defects

- investigations (OCT, ERG) possible

Exclusion Criteria:

- lesions within the optic nerve without extension in the optic tract

- neurological disease

- optic disc anomalies: glaucoma, nystagmus, high myopia

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Switzerland University Hospital Zurich Zurich

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ganglion cell thickness measurements will be taken at a minimum of 4 weeks after the inital diagnosis