Monitoring Anticoagulation in Patients on ECMO for Severe Lung Failure

Sponsor
University Hospital Ostrava (Other)
Overall Status
Completed
CT.gov ID
NCT06038682
Collaborator
(none)
100
1
33
3

Study Details

Study Description

Brief Summary

A monocentric observational study evaluates the accuracy of anticoagulation monitoring in critically ill patients on ECLS (extracorporeal life support) using new markers of the effect of direct thrombin inhibitors and also the accuracy of anticoagulation monitoring in patients on unfractionated heparin using anti-Xa. A more accurate setting of anticoagulation may lead to a reduction in the number of serious bleeding and thrombotic complications in these patients.

Condition or Disease Intervention/Treatment Phase

Detailed Description

Anticoagulation using a direct thrombin inhibitor, argatroban, is one of the modern options for anticoagulation in patients on VV (veno-venous) ECMO (extracorporeal membrane oxygenation) support, and in 2021 the ECMO center of the University Hospital Ostrava changed the standard anticoagulation using UHF (unfractionated heparin) to anticoagulation using Argatroban as a new standard of routine care. Argatroban shows more stable levels and has a short half-life, and a number of foreign ECMO centers have been using Argatroban for a long time also as basic anticoagulation in all ECMO patients.

To monitor the effect of direct thrombin inhibitors, it is possible to use monitoring of anti-FIIa activity, which directly assesses the effect of the anticoagulant on thrombin activity. Anticoagulation with Argatroban may reduce the risk of serious bleeding complications. Target values of aPTT (Activated Partial Thromboplastin Time) and anti-FIIa can be determined according to ELSO (Extracorporeal Life Support Organization) guidelines.

Study Design

Study Type:
Observational
Actual Enrollment :
100 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Monitoring Anticoagulation With Argatroban in Patients on Extracorporeal Membrane Oxygenation for Severe Lung Failure Using Anti-FIIa. Monitoring Anticoagulation With Unfractionated Heparin in Patients on Extracorporeal Membrane Oxygenation for Severe Lung Failure Using Anti-FXa.
Actual Study Start Date :
Apr 1, 2020
Actual Primary Completion Date :
Dec 31, 2022
Actual Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Argatroban anticoagulation

Study subjects in this group will receive Argatroban anticoagulation.

Drug: Argatroban Injection
Argatroban will be administered to the study subjects in this group in order to achieve anticoagulation.

Heparin anticoagulation

Study subjects in this group will receive Heparin anticoagulation.

Drug: Heparin
Heparin will be administered to the study subjects in this group in order to achieve anticoagulation.

Outcome Measures

Primary Outcome Measures

  1. Comparison of aPTT values with anti-IIa and Argatroban dose in patients on VV ECMO [up to 2 weeks]

    Comparison of correlation of aPTT and anti-IIa with dynamics of D dimer, FDP (fibrin degradation product) and acute phase reactants of ferritin, CRP (C-reactive protein) Correlation of bleeding complications with aPTT, anti-IIa, platelets

  2. Comparison of apt and anti-Xa values and heparin dose in patients on VV ECMO [up to 2 weeks]

    Comparison of correlation of aPTT and anti-Xa with dynamics of D dimer, FDP and acute phase reactants of ferritin, CRP

Secondary Outcome Measures

  1. Frequency and severity of bleeding complications [up to 2 weeks]

    Comparison of frequency and severity of bleeding complications in patients on anticoagulation with Argatroban and heparin

  2. Frequency and severity of thrombotic complications [up to 2 weeks]

    Comparison of frequency and severity of thrombotic complications in patients anticoagulated with Argatroban and heparin

  3. Consumption of blood products (in ml) [up to 2 weeks]

    The consumption of blood products (volume in ml) in patients on Argatroban and heparin

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Patients with COVID-19

  • ARDS according to the Berlin definition

  • Veno-venous (VV) ECMO

  • Full coagulation with Argatroban or heparin to an anti-FIIa value of 0.4-1.5 or aPTT 50-60

Exclusion Criteria:
  • age under 18 years

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Hospital Ostrava Ostrava Moravian-Silesian Region Czechia 70852

Sponsors and Collaborators

  • University Hospital Ostrava

Investigators

  • Principal Investigator: Filip BurÅ¡a, MD, Ph.D., University Hospital Ostrava

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University Hospital Ostrava
ClinicalTrials.gov Identifier:
NCT06038682
Other Study ID Numbers:
  • FNO-KARIM-Argatroban
First Posted:
Sep 15, 2023
Last Update Posted:
Sep 21, 2023
Last Verified:
Sep 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University Hospital Ostrava
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 21, 2023