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Anticoagulation with nadroparin in continuous venovenous hemofiltration (CVVH): extracorporeal clearance and systemic effects of nadroparin

Anticoagulation with nadroparin in continuous venovenous hemofiltration (CVVH): extracorporeal clearance and systemic effects of nadroparin - clearance and systemic effects of nadroparin in CVVH

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON29873
Enrollment
30
Registered
2006-12-04
Start date
2006-11-15
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

(anti)stolling acute renal failure renal replacement therapy

Interventions

None listed

Sponsors

Onze Lieve Vrouwe Gasthuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: non-surgical patients in the ICU with indication of CVVH for acute renal failure

Exclusion criteria

Exclusion criteria: severe liver failure active bleeding and need for transfusion

Design outcomes

Primary

MeasureTime frame
· anti-Xa activity in plasma and ultrafiltrate · sieving coefficient of anti-Xa · clearance of anti-Xa in relation to CVVH dose

Secondary

MeasureTime frame
The course of anti-Xa and ETP in plasma Relation between anti-Xa and ETP in plasma

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)