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Clinical Validation of the Norbert Health Device for Pulse Rate Measurement at Vigilant Clinical Testing

NCT06917352 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2025-06-10

No results posted yet for this study

Summary

The study will evaluate the measuring pulse rate (PR) using the Norbert Device (ND) as compared to a reference heart rate measured using an electrocardiogram (ECG).

Conditions

  • Healthy

Interventions

DEVICE

Norbert Device

The Norbert Device (ND) is a contactless, noninvasive device that provides measurements of pulse rate.

Sponsors & Collaborators

  • Vigilant Clinical Testing

    collaborator UNKNOWN

  • Norbert Health

    lead INDUSTRY

Principal Investigators

  • Tala Harake, Masters of Science · Vigilant Clinical Testing

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-04-11
Primary Completion
2025-04-13
Completion
2026-03-05
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 NCT06917352 on ClinicalTrials.gov