VENTRASSIST® exercise study in heart failure patients

Not Applicable

Completed

• Conditions: Exercise capacity; Cardiovascular - Other cardiovascular diseases

• Registration Number: ACTRN12608000106336
• Lead Sponsor: VENTRACOR Limited

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2008-02-27
• Study Completion: 2009-07-31
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 15

Inclusion Criteria

VentrAssist left ventricular assist device implanted, signed informed consent, age greater than or equal to 18 years, clinically stable as assessed by cardiologist, ambulatory

Exclusion Criteria

Active infection, exercise induced myocardial ischaemia or significant arrhythmias, inability to achieve a significant increase in left ventricular assist device flow without risk of suction as determined by clinical judgment, VENTRASSIST® left ventricular assist device implant duration less than 2 months

Study & Design

• Study Type: Observational
• Study Design: Not specified