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Visual Field Restoration in Patients With Post-stroke Homonymous Hemianopsia (REVOIR)

F

Fondation Ophtalmologique Adolphe de Rothschild

Status

Terminated

Conditions

Hemianopsia

Treatments

Other: stimulation of the blind visual field

Study type

Interventional

Funder types

NETWORK

Identifiers

NCT02886663
OGT_2015_16

Details and patient eligibility

About

This study will assess the effectiveness of a stimulus, in the blind field of hemianopsic patients, to restore the vision of patients with homonymous hemianopsia consecutive to stroke (unilateral occipital lesion). Hemianopsia occurs in 30% of strokes regardless of the cerebral localization and in 60% of stroke interesting the territory of the posterior cerebral artery.

Enrollment

9 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Presence of an homonymous visual field amputation after vascular retrochiasmatic lesion of the occipital region (visual cortex alone or with optical radiations or with other associated occipital areas)
  • inclusion 3 months to 36 months after stroke
  • Patients aged 18 years and older

Exclusion criteria

  • Brain injury history
  • Severe neuropsychological, psychiatric or behavioral disorder
  • Severe eye disorder or visual impairment (visual acuity less than 3/10)
  • Progressive eye disorder (cataracts or glaucoma)
  • insufficient French language proficiency to understand the questionnaires and rehabilitation tasks
  • patient under legal protection
  • patient's opposition to participate in the study
  • no medical insurance coverage
  • pregnant pr breastfeeding patient

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

9 participants in 2 patient groups

immediate rehabilitation
Experimental group
Treatment:
Other: stimulation of the blind visual field
delayed rehabilitation
Other group
Treatment:
Other: stimulation of the blind visual field

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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