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Data Collection With the P200TE and P200TxE

NCT05615896 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 5

Last updated 2024-03-12

No results posted yet for this study

Summary

The primary objective is to collect OCT scans on a modified P200TxE and P200TE.

Conditions

  • Retinal Disease

Interventions

DEVICE

Imaging Session

Various scans will be captured on both devices

Sponsors & Collaborators

  • Optos, PLC

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-04-22
Primary Completion
2021-04-28
Completion
2022-06-17
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 NCT05615896 on ClinicalTrials.gov