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Comparison of dialysate- and plasma clearences between three different haemodialysis modes.

Conditions
haemodialysis
treatment with artificial kidney
10038430
10038365
Registration Number
NL-OMON31119
Lead Sponsor
niversitair Medisch Centrum Sint Radboud
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
10
Inclusion Criteria

Dialysis patients > 18 years of age.
Dialysis > 3 months.
Signed informed consent.
Uncomplicated hemodialysis.
AV fistula with flow > 350ml/min.
Residual function < 1 ml/min.
Hemoglobin level between 6.8 - 8.3 mmol/l.
No bleeding tendency.

Exclusion Criteria

Instable dialysis
No bleeding tendency.
No informed consent.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Dialysate samples: Samples collected: continuously and separated in aliquots<br /><br>every hour.<br /><br>Phosphate, Cystatine C, Beta 2 Microglobuline, Vitamin B12, Urea, Creatinin.<br /><br><br /><br>Blood samples:<br /><br>Before start treatment: Haemoglobin, Haematocrit, Albumin, CRP.<br /><br><br /><br>Before and during treatment: Samples collected: before treatment, every hour<br /><br>and at treatment end.<br /><br>Before artificial kidney and just before venous return. (i.e. after post<br /><br>dilution substitution)<br /><br>Phosphate, Cystatine C, Beta 2 Microglobuline, Vitamin B12, Urea, Creatinin,<br /><br>Albumin, Haematocrit.<br /><br><br /><br>Once every type of treatment: D-dimeer en TAT as measures of degree of clotting<br /><br>in the artificial kidney. Before and after treatment.<br /><br>Anti- Xa as measure of activity of Nadoparin. Before and after treatment.<br /><br>C3D as measure of complement activation. After treatment. </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>- Diascan measurement on the Gambro AK 200-Ultra S. </p><br>
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