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Heartbeat Sensitivity Calibration Using the ECG Accessory

NCT01268007 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1

Last updated 2011-01-24

No results posted yet for this study

Summary

This is an observational, un-blinded, non-significant risk, non-interventional study designed to collect ECG data on at least one subject out of a pool of up to three (3) healthy male subjects at one clinical site (Clinical Trials of Texas). Cyberonics will be collecting ECG recordings collected by an investigational device for comparison with conventional ECG recordings. This data will be used to validate a new device under development.

Conditions

  • ECG Comparisons in Normal Healthy Subject

Sponsors & Collaborators

  • Cyberonics, Inc.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-12-31
Primary Completion
2010-12-31
Completion
2010-12-31

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 NCT01268007 on ClinicalTrials.gov