Side-by-Side Comparison of P200TE and Spectral OCT/SLO on Diseased Eyes

NCT02921568 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2017-03-14

No results posted yet for this study

Summary

This study is designed to evaluate and compare in-tissue performance of OCT scans on the new Optos P200TE, versus the predicate Optos Spectral OCT/SLO device.

Conditions

Interventions

DEVICE

P200TE

Optical Coherence Tomography and Scanning Laser Ophthalmoscope device.

DEVICE

Spectral OCT/SLO

Optical Coherence Tomography and Scanning Laser Ophthalmoscope device.

Sponsors & Collaborators

  • Optos, Inc.

    collaborator UNKNOWN
  • Optos, PLC

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-09-30
Primary Completion
2017-12-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT02921568 on ClinicalTrials.gov