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Use of Defibrillator Information in the Emergency Department

NCT00708058 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2012-03-20

No results posted yet for this study

Summary

This is a study to determine the feasibility of obtaining information stored in existing Medtronic internal defibrillators in patients who present to the Emergency Department(ED) for any reason. In addition, the study will determine if this information is useful to the ED physician in managing the patient's care, specifically as it relates to heart failure.

Conditions

  • Congestive Heart Failure
  • Medical Device

Sponsors & Collaborators

  • Ohio State University

    lead OTHER

Principal Investigators

  • Brian C Hiestand, MD · Ohio State University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-08-31
Primary Completion
2008-09-30
Completion
2010-03-31

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 NCT00708058 on ClinicalTrials.gov