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The effect of pump speed and a vessel dilating medication on the exercise capacity of patients with left ventricular assist devices (artificial heart pumps)

Phase 1
Recruiting
Conditions
heart failure
Cardiovascular - Other cardiovascular diseases
Registration Number
ACTRN12622001376730
Lead Sponsor
St Vincent's Hospital Sydney
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
16
Inclusion Criteria

•Willingness to give written informed consent and willingness to participate to and comply with the study.
•Age more or equal to 18 or legal guardian has signed consent
•Clinically stable
•Ambulatory
•More than 2 months after pump insertion

Exclusion Criteria

•Active infection
•Exercise induced myocardial ischaemia or significant arrhythmias
•Recent acute coronary syndrome (<6 weeks)
•Inability to achieve a significant increase in LVAD flow without risk of suction
•Estimated peak exercise load less than 30 watts
•Regular use of sildenafil

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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