Skip to content

Visual Field Restoration in Patients With Post-stroke Homonymous Hemianopsia

Visual Field Restoration in Patients With Post-stroke Homonymous Hemianopsia

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02886663
Acronym
REVOIR
Enrollment
9
Registered
2016-09-01
Start date
2016-12-13
Completion date
2019-11-25
Last updated
2019-12-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemianopsia

Brief summary

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.

Interventions

OTHERstimulation of the blind visual field

Sponsors

Fondation Ophtalmologique Adolphe de Rothschild
Lead SponsorNETWORK

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
change in the sensitivity of detection of a visual stimulus after rehabilitationchange from baseline sensitivity at week 22change in the mean number of points where the sensitivity is lower than 15db in each contralesional hemifield, before and after rehabilitation

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026