Study Comparing the P200TxE and P200DTx

NCT03964831 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2024-09-19

No results posted yet for this study

Summary

The study evaluates image quality between two devices.

Conditions

  • Retinal Disease

Interventions

DEVICE

P200TxE

The P200TxE ophthalmoscope provides widefield scanning laser ophthalmascope (SLO) fundus imaging.

DEVICE

P200DTx

The P200DTx ophthalmoscope provides widefield scanning laser ophthalmascope (SLO) fundus imaging.

Sponsors & Collaborators

  • Optos, PLC

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-06-18
Primary Completion
2020-01-14
Completion
2020-01-14
FDA Device
Yes

Countries

  • United States

Study Locations

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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 NCT03964831 on ClinicalTrials.gov