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Clinical Trials/NCT01509495
NCT01509495
Terminated
Phase 1

Impedance Measurements in Heart Failure Patients

Medtronic BRC3 sites in 3 countries20 target enrollmentDecember 2011
ConditionsHeart Failure

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Heart Failure
Sponsor
Medtronic BRC
Enrollment
20
Locations
3
Primary Endpoint
Impedance Measurement of Patients in Heart Failure, impedance change first to last measurement
Status
Terminated
Last Updated
11 years ago

Overview

Brief Summary

The purpose of this study is to measure impedance during inpatient treatment.

Registry
clinicaltrials.gov
Start Date
December 2011
End Date
May 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Medtronic BRC
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • patients admitted to hospital for symptoms of congestive heart failure
  • patients older than 18 years
  • patients willing and able to give informed consent

Exclusion Criteria

  • patients who will require adrenergic or positive inotropic medications
  • patients enrolled in a concurrent study that may confound the results of this study
  • patients unable or unwilling to participate in study procedures
  • patients who are pregnant
  • patients who are mentally handicapped or legal incompetent
  • patients who are dependent on investigator or sponsor

Outcomes

Primary Outcomes

Impedance Measurement of Patients in Heart Failure, impedance change first to last measurement

Time Frame: every 4 hours up to 48 hours

Secondary Outcomes

  • Correlation between hemodynamic (central venous or arterial pressure) and impedance measurements (optional)(every 4 hours up to 48 hours)
  • Accuracy of Respiratory rate determined by impedance measurements(every 4 hours up to 48 hours)

Study Sites (3)

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