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Pre- versus post-dilution haemofiltration: a prospective randomised cross-over study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN38768865
Enrollment
7
Registered
2005-07-06
Start date
2000-12-01
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute renal failure Urological and Genital Diseases Renal failure

Interventions

Continuous venovenous haemofiltration, predilution versus postdilution

Sponsors

Academic Medical Centre (Netherlands)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Eight critically ill patients with an indication for renal replacement therapy

Exclusion criteria

Exclusion criteria: Recent bleeding, treatment with aspirin within one week before inclusion or with therapeutic doses of unfractionated or low molecular weight heparin within 12 hours before inclusion or results of routine coagulation tests such as protrombin time (PT) and activated partial thromboplastin time (APTT) exceeding twice the upper limit of normal

Design outcomes

Primary

MeasureTime frame
Extracorporeal circuit survival time

Secondary

MeasureTime frame
Platelet activation, thrombin generation, urea clearance

Countries

Netherlands

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026