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Clinical Trials/NCT03505398
NCT03505398
Terminated
Not Applicable

Study of Visual-spatial Attention by Oculomotor Recording (Eye Tracking) as a Function of Central or Peripheral Visual Impairment

Nantes University Hospital1 site in 1 country71 target enrollmentMay 15, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Central or Peripheral Visual Impairment
Sponsor
Nantes University Hospital
Enrollment
71
Locations
1
Primary Endpoint
Microperimetry recording (central versus peripheral)
Status
Terminated
Last Updated
2 years ago

Overview

Brief Summary

The objective of this pilot work is to determine the role of central and peripheral visions in explicit attention processes (saccade planning) in the case of visual impairment.

Registry
clinicaltrials.gov
Start Date
May 15, 2018
End Date
June 20, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Male or female ≥18 years;
  • Patient with a central visual deficit (central scotoma on the visual field: DMLA, cones dystrophy ...) or peripheral (annular scotoma: chronic glaucoma, retinitis pigmentosa ...) or without visual deficit (corrected visual acuity and visual field)
  • Patient agreeing to participate in the study and signing informed consent
  • Patient affiliated to social security

Exclusion Criteria

  • Pregnant woman
  • Patient with known epilepsy
  • Major under judicial safeguard, or deprived of liberty
  • Major under guardianship or curatorship or admitted to a health or social institution for purposes other than research.

Outcomes

Primary Outcomes

Microperimetry recording (central versus peripheral)

Time Frame: Day 0

recording of automated visual field (central versus peripheral)

Time Frame: Day 0

Measurement of visual acuity (central versus peripheral)

Time Frame: Day 0

recording of eye movements (central versus peripheral)

Time Frame: Day 0

Secondary Outcomes

  • recording of automated visual field (patient versus control)(Day 0)
  • Microperimetry recording (patient versus control)(Day 0)
  • recording of eye movements (patient versus control)(Day 0)
  • Measurement of visual acuity (patient versus control)(Day 0)

Study Sites (1)

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