Skip to content

Thrombin Generation after Abrupt Cessation versus Weaning over 8 hours of Continuous Infusion of Unfractionated Heparin in ICU-patients after Discontinuation of Continuous Venovenous Hemofiltration (CVVH).

Thrombin Generation after Abrupt Cessation versus Weaning over 8 hours of Continuous Infusion of Unfractionated Heparin in ICU-patients after Discontinuation of Continuous Venovenous Hemofiltration (CVVH). - Heparin Rebound

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON29772
Enrollment
20
Registered
2006-08-22
Start date
2006-06-01
Completion date
Unknown
Last updated
2024-06-18

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

Conditions

preventie van thrombose prevention of thrombosis thrombosis prophylaxis

Interventions

In one group of patients Heparin infusion will be stopped simultaneous to stopping of CVVH. In the other group of patients UFH infusion will be reduced to 50% from the previous infusion rate. After

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients scheduled to stop treatment with CVVH because they no longer require it (physicians discretion / local protocol) Age >18 years At least 48 hours of CVVH treatment with concomitant continuous infusion of UFH At least 36 hours of continuous UFH infusion in the last 48 hours prior to inclusion

Exclusion criteria

Exclusion criteria: Patients with known coagulation disorders Patients receiving any anti-coagulant treatment for reasons other than CVVH

Design outcomes

Primary

MeasureTime frame
Markers of coagulation and fibrinolysis: aPTT, anti-Xa, factor VII/VIIa, TF, TFPI-antigen, TFPI activity, protein C / activated protein C, prothrombine fragment 1.2, TATc, ETP (Endogenous Thrombin Potential), Fibrin monomers, soluble thrombomodulin, PAPc, PAI.

Secondary

MeasureTime frame
-

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)