Amblyopia Clinical Trial
Official title:
MEPEDS New Device Pediatric Vision Scanner
Verified date | October 2012 |
Source | Rebiscan, Inc. |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Food and Drug Administration |
Study type | Observational |
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.
Status | Completed |
Enrollment | 32 |
Est. completion date | June 2011 |
Est. primary completion date | June 2011 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 6 Months to 6 Years |
Eligibility |
Inclusion Criteria: - Children aged 6 months to 6 years - Signed Informed consent by parent or guardian - Meet all inclusion criteria. Exclusion Criteria: - Children with a history of developmental delay or cognitive deficit - Children unable to complete the GSE (including visual acuity testing) |
Observational Model: Case Control, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
United States | Doheny Eye Institute | Los Angeles | California |
Lead Sponsor | Collaborator |
---|---|
Rebiscan, Inc. | University of Southern California |
United States,
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. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Binocularity score | Day 1 | Yes | |
Secondary | Presence of amblyopia risk factors | Day 1 | Yes |
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