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.
Investigators
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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