Feasibility of a Video-oculography in Patients With Huntington's Disease VOG-HD Study

University Hospital, Angers

Status: Unknown

Conditions: Huntington Disease

Treatments: Device: Eye-tracking

Study type: Interventional

Funder types: Other

Identifiers

NCT02563418

AOI 2013 - 11

Details and patient eligibility

About

The purpose of this study is to know the limits of feasibility of a reliable oculomotor record for patient with Huntington's disease.

Enrollment: 60 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Corrected visual acuity >1/10
• Aged over 18 years
• Patient with the mutation that is to say the presence of an abnormal number of trinuclide: CAG> 38 in the first exon of the huntingtin gene.
• Total Functional Capacity Scale (CFT) ≥ 3

Exclusion criteria

• Patients or trustworthy person who have not given their written consent, informed and signed.
• Patients are not affiliated or who are not entitled to Social Security
• Private patients of liberty by administrative or judicial decision, or patients supervision
• Associated disease with neurological repercussions

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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60 participants in 1 patient group

Patient with Huntington's disease

Experimental group

Treatment:

Device: Eye-tracking