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

Not Applicable

• Conditions: Huntington Disease

• Registration Number: NCT02563418
• Lead Sponsor: University Hospital, Angers

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study Start: 2014-05
• Status Verified: 2015-09
• Study First Submitted: 2015-09-08
• Study First Submitted QC: 2015-09-29
• Last Update Submitted: 2015-09-29
• Study First Posted: 2015-09-30
• Last Update Posted: 2015-09-30
• Primary Completion: 2017-05

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 60

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
saccadic measures with the eye tracker	1 day	one measure in the evening and one in the afternoon

Trial Locations

Locations (1)

Centre Hospitalier Universitaire; 🇫🇷 Angers, France