Impact of Hemodynamic Ramp Test-Guided HVAD RPM and Medication Adjustments on Exercise Tolerance and Quality of Life
Trial ID or NCT#
Status
Purpose
The main purpose of this study is to compare Echo-guided testing to the Hemodynamic-Echo Ramp Tests to determine which method of testing provides better information for adjusting pump speed and medical treatment for Left Ventricular Assist Device (LVAD) patients. Better adjustments may provide better quality of life, exercise tolerance and reduced unwanted cardiac events over a 6-month period.
Official Title
Impact of Hemodynamic Ramp Test-Guided HVAD RPM and Medication Adjustments on Exercise Tolerance and Quality of Life: A Multicenter Study
Eligibility Criteria
- 1. Patient older than 18 years 2. Newly implanted HVAD 3. HVAD support anticipated for at least 6 months 4. Patient is ambulatory and discharged from hospital without inotropes 5. Patient is between 1 and 3 months post implant 6. Patient has not had a right heart catheterization since discharged from HVAD implantation hospitalization
- 1. The current HVAD is a replacement device 2. Patients currently has Right Ventricle (RV) failure requiring home inotropes 3. Inability to preformed right heart cath 4. Inadequate echocardiographic windows
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Contact
Dip Banerjee, MD
View on ClinicalTrials.gov