Feasibility of a Video-oculography in Patients With Hunti... | NCT02563418

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

NCT02563418

Sponsor

University Hospital, Angers

Status

Unknown status

Last Update Posted

Sep 30, 2015Estimated

Enrollment

60Estimated

Phase

Not Applicable

Conditions

Huntington Disease

Interventions

Eye-tracking

Countries

France

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

Status Module

Record Verification Date

Sep 2015

Overall Recruitment Status or Expanded Access Status

Unknown status

Last Known Status

Recruiting

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

May 2014

Primary Completion Date

May 2017Estimated

Completion Date

Not provided

First Submitted Date

Sep 8, 2015

First Submission Date that Met QC Criteria

Sep 29, 2015

First Posted Date

Sep 30, 2015Estimated

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

Sep 29, 2015

Last Update Posted Date

Sep 30, 2015Estimated

Description Module

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 provided

Design Module

Study Type

Interventional

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Not provided

Target Follow-Up Duration

Not provided

Phases

Not Applicable

Interventional Study Design

Allocation

Biospecimen

No data available

No data is available for this block.

Enrollment

60Estimated

Label	Type	Description	Intervention Names
Patient with Huntington's disease	Experimental		Device: Eye-tracking

Name	Type	Description	Arm Group Labels	Other Names
Eye-tracking	Device		Patient with Huntington's disease

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
saccadic measures with the eye tracker	one measure in the evening and one in the afternoon	1 day

Secondary Outcomes

Not provided

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

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

Accepts Healthy Volunteers

Sex

All

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

18 Years

Maximum Age

Not provided

Standard Ages

AdultOlder Adult

Study Population

Not provided

Sampling Method

Not provided

Contacts/Locations Module

Central Contacts

Name	Role	Phone	Extension	Email
Sophie Hue	Contact	33 (0)241353800		sophie.hue@chu-angers.fr

Overall Officials

Not provided

Locations

Facility	Status	City	State	ZIP	Country	Contacts
Centre Hospitalier Universitaire	Recruiting	Angers		49000	France

Condition Browse Module

MeSH Terms

ID	Term
D006816	Huntington Disease

Ancestor Terms

ID	Term
D001480	Basal Ganglia Diseases
D001927	Brain Diseases
D002493	Central Nervous System Diseases
D009422	Nervous System Diseases

Browse Leaves

Not provided

Browse Branches

Not provided

Intervention Browse Module

MeSH Terms

ID	Term
D000084542	Eye-Tracking Technology

Ancestor Terms

ID	Term
D053483	Eye Movement Measurements
D003941	Diagnostic Techniques, Ophthalmological
D019937	Diagnostic Techniques and Procedures
D003933	Diagnosis

Browse Leaves

Not provided

Browse Branches

Not provided