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Gated 13N-NH3 PET before and during hemodialysis for the assessment of changes in myocardial perfusion, volumes and output of the left ventricle.

Recruiting
Conditions
10082206
cardiac perfusion
left ventricular function
Registration Number
NL-OMON30270
Lead Sponsor
niversitair Medisch Centrum Groningen
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
8
Inclusion Criteria

1) Adult (age equal to/above 18) HD patients who have been treated with HD for at least six months. 2) Patients must have an arterio-venous fistula without recirculation established by Transonic flow measurements.

Exclusion Criteria

1. The absence of informed consent (see ethical considerations). 2. The need to perform HD with pre-dilution. 3. Recent haemorrhage. 4. Unstable angina pectoris. 5. History of myocardial infarction. 6. Inability to endure a horizontal position for a longer period of time. 7. Arrhythmia. 8. The use of long-acting nitrates. 9. Left ventricular ejection fraction <= 30%. 10. Diabetes Mellitus. 11. Pregnancy or suspicion hereof.

Study & Design

Study Type
Observational invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The outcome parameters are changes in cardiac output, myocardial contractility,<br /><br>left ventricular ejection fraction, left ventricular diameter, left ventricular<br /><br>end-systolic volume, left ventricular end-diastolic volume, left ventricular<br /><br>myocardial perfusion in ml/min/g and regional wall motions. Data will be<br /><br>analysed quantitatively and displayed in a 17-segment polar map. Each<br /><br>individual session will be evaluated for pre- and post-study body weight, total<br /><br>ultrafiltration volume, blood pressure and the course of relative blood volume<br /><br>(measured non-invasively by an RBV monitor) throughout the study. </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>n.a.</p><br>
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