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Refraction Determination Analysis

L

Lee, Steven, M.D.

Status

Completed

Conditions

Astigmatism,
Eye Strain,
Presbyopia,
Hyperopia,
Myopia,

Treatments

Device: Traditional refraction
Device: Telemedicine refraction

Study type

Interventional

Identifiers

NCT01995435
SPL-321-REF

Details and patient eligibility

About

Correlating the accuracy of a refraction done over telemedicine to that of a standard refraction, with a study hypothesis that the results will be equivalent.

Enrollment

30 patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18-40 years old
  • healthy eyes

Exclusion criteria

  • mid level ocular diseases (glaucoma, hypertension, retinal issues)
  • psychiatric disorders
  • brain tumor or history of
  • under 18, or over 40 years old

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

30 participants in 2 patient groups

Telemedicine refraction before traditional refraction
Experimental group
Description:
We will first refract an individual using telemedicine refraction, and then refract them using a traditional refraction method.
Treatment:
Device: Telemedicine refraction
Device: Traditional refraction
Traditional refraction before telemedicine refraction
Experimental group
Description:
We will first refract an individual using a traditional refraction, and then refract them using a telemedicine refraction method.
Treatment:
Device: Telemedicine refraction
Device: Traditional refraction

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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