Inter-Device Reliability of the NPi-300 Pupillometer

NCT04993833 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 70

Last updated 2022-09-30

No results posted yet for this study

Summary

The purpose of this study is to explore the inter-device reliability between the NPi-200 and NPi-300.

Conditions

Interventions

DEVICE

NPi-200 and NPi-300 pupillometers

Device which measures PLR.

Sponsors & Collaborators

  • NeurOptics Inc.

    collaborator INDUSTRY
  • University of Texas Southwestern Medical Center

    lead OTHER

Principal Investigators

  • DaiWai M Olson, PhD · University of Texas Southwestern Medical Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-08-25
Primary Completion
2022-08-31
Completion
2022-08-31
FDA Device
Yes

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 NCT04993833 on ClinicalTrials.gov