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Clinical Research Directory

Browse clinical research sites, groups, and studies.

5 clinical studies listed.

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Visual Field Defect

Tundra lists 5 Visual Field Defect clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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NOT YET RECRUITING

NCT07427719

Retinopathy of Prematurity - Visual Function and Retinal Structure

Children born prematurely may develop a characteristic retinal disease named retinopathy of prematurity (ROP). This disease could lead to retinal detachment and blindness. ROP was traditionally treated with laser, but injection with a medication (A-VEGF) has become more common. In this study, the researchers will explore whether treatment of ROP affects visual function and retinal development. To explore this, the study group will examine children with ROP (but not treated) with children treated with either laser or injection. The researchers will compare the children's visual functions (e.g. visual acuity and visual field) and their retinas (e.g. central and peripheral retina).

Gender: All

Ages: 6 Years - 20 Years

Updated: 2026-02-23

1 state

Retinopathy of Prematurity (ROP)
Prematurity Complications
Cerebral Visual Impairment
+1
NOT YET RECRUITING

NCT06875206

Visual Restoration Using Focused Ultrasound Stimulation and Immersive Virtual Reality After Stroke

This research will explore if brain stimulation combined with virtual reality therapy improves visual impairment. The stimulation technique is called low-intensity focused ultrasound stimulation (LIFUS). The treatment uses ultrasound to stimulate vision specific parts of the brain. Before this therapy, the participants will get structural brain imaging. Functional brain imaging will be performed before and after the study's completion to measure brain activity response to therapy. The purpose of this research study is to evaluate patients who have had a stroke between 6 and 24 months ago with a visual field impairment. The duration of active participation in the study is 1.5 months.

Gender: All

Ages: 18 Years - Any

Updated: 2026-02-20

1 state

Stroke
Visual Field Defect
Visual Field Defect Following Cerebrovascular Accident
+4
ACTIVE NOT RECRUITING

NCT06920290

Visual Field Analysis With Artificial Intelligence

The purpose of this study is to analyze visual field data from healthy participants. This data will be used to develop and optimize a new visual field perimeter test. The test will incorporate an advanced algorithm, which may include the use of Artificial Intelligence (AI), to enhance accuracy and efficiency in identifying test points.

Gender: All

Ages: 18 Years - 100 Years

Updated: 2025-11-03

1 state

Glaucoma
Visual Field Defect
RECRUITING

NCT07105358

Visual Plasticity Following Brain Lesions

The VIBRANT (Vision Improvement through Behavioral Rehabilitation And Neuroplasticity Training) study is a prospective, double-blind, crossover design (within-subject) in participants with homonymous hemianopia-a type of visual field loss resulting from damage to the post-chiasmatic visual pathways. It aims to investigate whether transcranial random noise stimulation (tRNS) combined with perceptual learning-based training has potential for improving visual impairments.

Gender: All

Ages: 18 Years - Any

Updated: 2025-08-05

1 state

Visual Field Defect
Stroke
Hemianopia
+5
NOT YET RECRUITING

NCT05703360

Effectiveness of AV-stimulation in Immersive VR to Improve Visual Perception and Driving Performance

The goal of this clinical trial is to evaluate the effectiveness of an immersive virtual-reality (IVR) based stimulation program, in improving visual perception for people who have lost their driver's license due to perceptual or cognitive impairments. The main questions it aims to answer are: 1. Can the 6-week IVR stimulation program help improve driving performance? 2. Will participants experience improvement in visual detection and perception after training? Study Design Summary: * Participants will be randomized into a waitlist group or intervention-first group * The VR-based intervention will consist of training every 2 days for six weeks * Waitlist group will wait 6 weeks before starting intervention at study midpoint (week 7) * Intervention-first group will begin with intervention (week 1-6) and then stop intervention at study midpoint * Participants will complete tests related to driving performance, visual attention, and visual fields at the start of study, midpoint, and end of study Researchers will analyze data for changes from baseline in outcome measures.

Gender: All

Ages: 25 Years - Any

Updated: 2024-12-19

1 state

Stroke
Visual Impairment
Low Vision
+6