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CompletedNCT02003235Updated Jul 21, 2017

Assessment of Device for Treatment of Amblyopia

An interventional study of Daily watching videos using Reviview™, a dichoptic video display device, for 60 min in Amblyopia, sponsored by Visior Technologies Ltd.. Completed at 1 site in Israel. Open to participants aged 4 Years to 8 Years. Per ClinicalTrials.gov, last updated 2017-07-21.

Sponsored by Visior Technologies Ltd. · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
35
Allocation
Not applicable
Ages
4 Years to 8 Years
Sex
All
01

Study summary

The study will evaluate the effect of Reviview™, a dichoptic video display device for administrating a novel treatment protocol for Amblyopia (lazy eye) in kids.

The effect of the treatment will be measured by the change from baseline in Visual acuity and in Stereoscopic Vision; and to assess the ease of use of and compliance by the patients.

02

Conditions studied

  • Amblyopia

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Keywords

  • Amblyopia
03

In context

Amblyopia

183 studies on the registry are indexed under Amblyopia; 43 are open to participants now.

This study's enrollment of 35 is below the median of 60 across 133 interventional studies indexed under Amblyopia.

Browse Amblyopia studies →

Lead sponsor

Visior Technologies Ltd. is the lead sponsor of 3 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
4 Years to 8 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

Refractive or Strabismic Amblyopia, with best corrected visual acuity.

(1) Refractive Amblyopia, visual acuity score \<6:15 (worse then)

  • or (2) Strabismic Amblyopia, visual acuity score between 6:15 and 6:30

Exclusion criteria

Exclusion Criteria:

Diagnosed with epilepsy, recently treated with occlusion or penalization therapy

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
35 participants (actual)

Study arms

  • Experimental
    Single Arm

    Daily watching videos using Reviview™, a dichoptic video display device

    Device: Daily watching videos using Reviview™, a dichoptic video display device, for 60 min

Interventions

  • DeviceDaily watching videos using Reviview™, a dichoptic video display device, for 60 min
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What researchers measure

Primary outcomes

  1. Improvement in VA in amblyopic eye

    Time frame: 3 months

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Study locations

1 site
  • Tel-Aviv Sourasky Medical Center
    Tel-Aviv, Israel
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 21, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02003235
Lead sponsor
Visior Technologies Ltd.
Responsible party
Sponsor
First posted
Dec 6, 2013
Start date
Oct 2013
Primary completion
Jul 15, 2017
Completion
Jul 15, 2017
Last update
Jul 21, 2017

Study contacts

Haim Stolovitch, MD
principal investigator · Tel-Aviv Sourasky Medical Center

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2017. You cannot join it, but the record below documents what was studied.

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