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Refraction Determination Analysis

NCT01995435 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2015-09-07

No results posted yet for this study

Summary

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.

Conditions

  • Myopia,
  • Hyperopia,
  • Astigmatism,
  • Presbyopia,
  • Eye Strain,

Interventions

DEVICE

Telemedicine refraction

DEVICE

Traditional refraction

Sponsors & Collaborators

  • Lee, Steven, M.D.

    lead INDIV

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
TRIPLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-02-28
Primary Completion
2015-06-30
Completion
2015-06-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01995435 on ClinicalTrials.gov