Amblyopia and Strabismus Detection Using a Pediatric Vision Scanner
MEPEDS New Device Pediatric Vision Scanner
1 other identifier
observational
32
1 country
1
Brief Summary
The purpose of this project is to compare the performance of the Pediatric Vision Scanner (PVS) with the Gold Standard Examination to determine the effectiveness of the PVS at detecting amblyopia and strabismus. All tests and observations will be done at a single visit over the course of approximately 30 minutes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jan 2011
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2011
CompletedFirst Submitted
Initial submission to the registry
October 5, 2012
CompletedFirst Posted
Study publicly available on registry
October 15, 2012
CompletedOctober 15, 2012
October 1, 2012
5 months
October 5, 2012
October 12, 2012
Conditions
Outcome Measures
Primary Outcomes (1)
Binocularity score
Day 1
Secondary Outcomes (1)
Presence of amblyopia risk factors
Day 1
Study Arms (3)
Normal Controls
Structurally normal eye with equal visual acuity and normal stereopsis.
Referral required
Diagnosed with amblyopia or constant strabismus, categorized based on the GSE. Amblyopia: * VA \<20/40 and 2 logMAR lines difference in normal eye * Mild amblyopia (\>20/40) * Moderate amblyopia (20/40 and \<20/100) * Severe amblyopia (≥20/100 or worse) * Bilateral amblyopia: \>4 years age VA\<20/40 OU including high hyperopia or high astigmatism. Strabismus: * Constant: \>2 PD at near and or distance. * Intermittent: strabismus that could be controlled intermittently either through fusional mechanisms or a compensatory head position. Amblyogenic factor categorization: * 'Anisometropia'- (1.5 Diopters (D) or more difference in refractive error between the two eyes. * 'hypermetropia' (≥3.5 D), * 'myopia' (≥-4.0 D), * 'astigmatism' (≥1.5 D). * 'structural abnormalities' of the eye will not be excluded, but will be considered to have vision loss if visual acuity is 20/40 or worse.
Borderline
(no long-term harm to patient if referral is delayed, however the patient does have conditions that might benefit from monitoring): Equal visual acuity and no structural abnormality with any of the following: Amblyogenic factor, intermittent strabismus, structural abnormalities, refractive error, reduced stereopsis.
Interventions
Subject is scanned with a 2.5 second pediatric vision scanner device test.
Eligibility Criteria
Children presenting for ophthalmic exam at eye clinic.
You may qualify if:
- Children aged 6 months to 6 years
- Signed Informed consent by parent or guardian
You may not qualify if:
- Children with a history of developmental delay or cognitive deficit
- Children unable to complete the GSE (including visual acuity testing)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Rebiscan, Inc.lead
- University of Southern Californiacollaborator
Study Sites (1)
Doheny Eye Institute
Los Angeles, California, 90033, United States
Related Publications (1)
Loudon SE, Rook CA, Nassif DS, Piskun NV, Hunter DG. Rapid, high-accuracy detection of strabismus and amblyopia using the pediatric vision scanner. Invest Ophthalmol Vis Sci. 2011 Jul 7;52(8):5043-8. doi: 10.1167/iovs.11-7503.
PMID: 21642624BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Rohit Varma, MD, PhD
University of Southern California
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 5, 2012
First Posted
October 15, 2012
Study Start
January 1, 2011
Primary Completion
June 1, 2011
Study Completion
June 1, 2011
Last Updated
October 15, 2012
Record last verified: 2012-10