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NCT02422160 Clinical Trial

Vision Outcomes Using Quantitative Optical Coherence Tomography Evaluation in Age Related Macular Degeneration

Age-Related Macular Degeneration Clinical Trial

Official title:
Vision Outcomes Using Quantitative Optical Coherence Tomography Evaluation in Age Related Macular Degeneration

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02422160
Other study ID # 33624
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 2015
Est. completion date December 2021

Study information
Verified date May 2022
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The investigators have developed an image analysis method that can predict the likelihood that a patient with age related macular degeneration (AMD) will progress within 1 year, based on computerized analysis of optical coherence tomography (OCT) images that are routinely acquired in clinical practice on each patient visit to the ophthalmologist. The investigators' goal is to evaluate whether this method will improve the ability to detect AMD earlier and improve visual outcomes in AMD patients by assigning patient risk categories and having patients come back for follow up based on those categories.

Recruitment information / eligibility
Status Completed
Enrollment 28
Est. completion date December 2021
Est. primary completion date December 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Non-exudative age-related macular degeneration Exclusion Criteria: - Exudative age-related macular degeneration

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• No interventions are planned
No interventions are planned

Locations
Country Name City State
United States Byers Eye Institute at Stanford Palo Alto California

Sponsors (1)
Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Visual Acuity Two Years
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