MedPath

Portable Autorefractor- InstaRef R20

Not yet recruiting
Conditions
to assess refractive error
Registration Number
CTRI/2021/11/037869
Lead Sponsor
Diwakar Rao
Brief Summary

This is a Prospective Study, which is validating a Portable Autorefractor (InstaRef R20) comparing against Subjective refraction (gold standard),Open field AR, Plusoptix, Quciksee, Standard tabletop autorefractor Topcon ARK 800 and Cycloplegic refraction. This device uses a Shack Hartmann aberrometer technology, which is used to find a Refractive error,and has a distinct advantage of not only being affordable and portable but can also be used as a standalone device.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
132
Inclusion Criteria
  • Subjects with BCVA 20/20 in each eye.
  • Subjects with refractive errors between Sph+/-10D, Cyl +/-5D.
Exclusion Criteria
  • Subjects with significant media opacity- corneal opacity, advanced cataract, vitreous hemorrhage.
  • posterior segment pathology affecting visual acuity, amblyopia and inability to fixate, active eye infection, inflammation.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Demonstrate the performance of InstaRef R20 when compared against subjective refraction (gold standard).At the end of the study
Secondary Outcome Measures
NameTimeMethod
Demonstrate the substantial equivalence in terms of performance and safety of a InstaRef R20 in measuring refractive errors when compared against a Open field AR, Plusoptic, Quicksee and standard tabletop autorefractor Topcon ARK 800.

Trial Locations

Locations (1)

Sankara Eye Hospital

🇮🇳

Bangalore, KARNATAKA, India

Sankara Eye Hospital
🇮🇳Bangalore, KARNATAKA, India
Diwakar Rao
Principal investigator
9972015862
dot_diwakar@yahoo.co.in

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