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OpenTrials
Completed

NCT Number: NCT05286502

NW500 Non-Mydriatic Retinal Camera Clinical Performance Study

Comparison of color fundus images acquired by the Topcon NW500 non-mydriatic retinal camera (investigational device) and the Topcon TRC-NW400 (predicate device)

Completed

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Key information

Conditions

Fundus Photography

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Topcon Healthcare Solutions

Oakland, New Jersey, 07436, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects who are 18 years of age or older on the date of informed consent.
  • Subjects who are able to understand the written informed consent and are willing to participate as evidenced by signing the informed consent.

Exclusion criteria

  • Subjects who are unable to tolerate ophthalmic imaging.
  • Subjects with poor fixation or ocular media not sufficiently clear to obtain acceptable images.
  • Subjects who cannot follow instructions to complete the required testing.

Treatment and study plan

Fundus Photography

Device

color fundus photography

Primary outcomes

  1. fundus photo image quality

    Time frame: 1 day

Sponsors and collaborators

Lead sponsor

Topcon Corporation

Industry

Registry information

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Mar 18, 2022
Registry last updated
Jun 8, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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