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Optivol Diagnostic Data for Discharge in Heart Failure

NCT00420108 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 23

Last updated 2010-08-20

No results posted yet for this study

Summary

The objective of this study is to evaluate whether the heart rate variability, daily heart rate, and/or intrathoracic impedance recorded by implantable cardiac devices can be used in conjunction with other traditional clinical practice methods to determine if heart failure patients are ready for hospital discharge.

Conditions

  • Heart Failure, Congestive
  • Cardiac Pacemaker, Artificial

Sponsors & Collaborators

  • Medtronic

    collaborator INDUSTRY

  • Thomas Jefferson University

    lead OTHER

Principal Investigators

  • David J Whellan, MD MHS · Thomas Jefferson University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-12-31
Primary Completion
2010-02-28
Completion
2010-02-28

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT00420108 on ClinicalTrials.gov