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Evaluation Of The GE Monitor Product Line

NCT00730119 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2017-08-08

No results posted yet for this study

Summary

This investigation is a multi-center study that will demonstrate that the GE Monitor meets equivalency and/or accuracy and/or performance criteria. This investigation will compare the test device(s) to itself, or one of the reference parameters, or a combination of parameters, including NIBP, temperature, SpO2, respirations, and ECG.

Conditions

  • Non-invasive Blood Pressure
  • Temperature
  • SpO2
  • Respiration
  • ECG

Sponsors & Collaborators

  • GE Healthcare

    lead INDUSTRY

Principal Investigators

  • Jean D Sesing · GE Healthcare

Eligibility

Min Age
1 Minute
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2001-10-31
Primary Completion
2010-03-31
Completion
2010-05-31

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 NCT00730119 on ClinicalTrials.gov