Optical Coherence Tomography (OCT) Data Collection Study

Optical Coherence Tomography Data Collection Study

Collect OCT data to evaluate the range and age trend of eye measurements.

Study Overview

• Status: Completed
• Conditions: No Eye Disease

• Study Type: Observational
• Enrollment (Anticipated): 400

Contacts and Locations

Study Locations

• United Kingdom
  • England
    • London, England, United Kingdom, EC1V 9EL
      • Institute of Ophthalmology, University College London
• United States
  • California
    • Fullerton, California, United States, 92831
      • Southern California College of Optometry
    • Pomona, California, United States, 91766
      • College of Optometry, Western University of Health Sciences
    • San Jose, California, United States, 95112
      • Buena Vista Eye Care
  • Illinois
    • Chicago, Illinois, United States, 60616
      • Illinois Eye Institute

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

• Sampling Method: Non-Probability Sample

Study Population

No eye disease

Description

Inclusion Criteria:

• At least 18 years of age
• Able and willing to provide consent
• Able and willing to complete the required examininations and visit
• Refractive error within 8 diopters sphere and within 2 diopters cylinder in each eye
• Best corrected visual acuity of 20/30 or better in each eye

Exclusion Criteria:

• History of leukemia, AIDS, dementia or multiple sclerosis
• Concomitant use of hydroxycloroquine or chloroquine
• Family history of glaucoma among first degree relatives
• Intraocular pressure of 22mm Hg or greater in either eye
• Unreliable or abnormal visual field
• Active ocular disease
• Previously diagnosed with glaucoma or glaucoma suspect
• Congenital ocular abnormalities
• Previous intra-ocular surgery or laser treatment (other than refractive surgery or uncomplicated cataract surgery greater than 6 months previously)
• Anatomic narrow angle

Study Plan

How is the study designed?

Number of groups / cohorts

6

Cohorts and Interventions

Group / Cohort
Age 18-29
Age 30-39
Age 40-49
Age 50-59
Age 60-69
Age 70+

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
range of eye measurements	Day 1

Secondary Outcome Measures

Outcome Measure	Time Frame
age trend of eye measurements	Day 1

Collaborators and Investigators

• Sponsor: Optovue
• Investigators: Principal Investigator: George Comer, OD, MBA, Southern California College of Optometry at Marshall B. Ketchum University; Principal Investigator: Michael Chaglasian, OD, Illinois Eye Institute; Principal Investigator: Jorge Cuadros, OD, PhD, Buena Vista Eye Care; Principal Investigator: David Garway-Heath, MD, Institute of Ophthalmology, University College London; Principal Investigator: Pinakin G Davey, OD, PhD, Western University of Health Sciences

Study record dates

Study Major Dates

• Study Start: September 1, 2011
• Primary Completion (Actual): March 1, 2012
• Study Completion (Actual): March 1, 2012

Study Registration Dates

• First Submitted: October 23, 2011
• First Submitted That Met QC Criteria: October 24, 2011
• First Posted (Estimate): October 26, 2011

Study Record Updates

• Last Update Posted (Estimate): May 2, 2012
• Last Update Submitted That Met QC Criteria: May 1, 2012
• Last Verified: May 1, 2012

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Eye Diseases
• Other Study ID Numbers: OCT 200-47091