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Completed

NCT Number: NCT03208270

Antithrombin Supplementation in ECMO

Bleeding is the most feared complication during extracorporeal membrane oxygenation (ECMO) and is associated with high dosing of heparin. There is no consensus on antithrombin (AT) supplementation during ECMO. However, AT is needed by heparin to properly anticoagulate. We hypothesize that maintaining normal antithrombin levels during ECMO is associated with a less heparin dosing and more adequate level of anticoagulation.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

Milan, MI, 20122, Italy

About this study

Extracorporeal membrane oxygenation (ECMO) is a life support for patients with severe acute respiratory failure when conventional treatments failed but it is accompanied by a significant risk of bleeding. Heparin is required during ECMO to avoid circuit thrombosis and its anticoagulant effect is strictly dependent on antithrombin (AT). AT also plays a central role in mediating inflammation. Acquired AT deficiency is common in patients on ECMO, arguably due to long term anticoagulation in addition to sepsis itself. Guidelines suggest to supplement AT in ECMO only when its deficiency coexists with heparin resistance. Few studies evaluated the effect of AT supplementation during ECMO without a consensus on the appropriate level to be maintained. AT supplementation increase anti-Factor Xa (anti-Xa) levels without increasing heparin dosage. This may have a clinical impact because risk of bleeding during ECMO is associated with higher heparin dosage.

We hypothesize that maintaining normal antithrombin activity levels (80%-120%) during ECMO is associated with: I. less heparin dosage, II. a more adequate level of anticoagulation, III. less hemostasis related complications, and IV. a lower level of inflammation.

Adult patients on veno-venous ECMO for respiratory failure will be randomized to maintain AT between 80% and 100% (study group) or no supplementation unless heparin resistance occurs (control group). Sample size of at least 20 patients per group (n=40) is calculated upon the primary outcome measure of reduction of heparin use in the study group compared to the control group. AT and anti-Xa will be measured before ECMO and daily while on ECMO. Anticoagulation will be guaranteed with unfractionated heparin infusion with a target aPTT 1.5-2X normal. Study will end at ECMO removal.

Consistent literature suggests that current ECMO anticoagulation strategies are suboptimal probably due to improper antithrombin supplementation. A normal antithrombin level could guarantee an adequate anticoagulation regimen.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • patients requiring veno-venous ECMO for severe respiratory failure.

Exclusion criteria

  • patients with pre-existent heparin-induced thrombocytopenia

Treatment and study plan

Antithrombin supplementation

Drug

antithrombin concentrate will be supplemented to maintain a functional antithrombin level between 80%-120%

Other names: Antithtrombin

No antithrombin supplementation

Drug

supplementation of antithrombin will not be provided unless "heparin resistance" occurs

Other names: No antithrombin

Primary outcomes

  1. Amount of heparin

    Time frame: through study completion, an average of 10 days

    Heparin dosage to maintain aPTT ratio between 1.5-2

Secondary outcomes

  1. Bleeding

    Time frame: through study completion, an average of 10 days

    Bleeding complications

  2. Adequacy of anticoagulation

    Time frame: through study completion, an average of 10 days

    Adequacy of anticoagulation, assessed through Anti-Xa levels

  3. thrombosis

    Time frame: through study completion, an average of 10 days

    Patient's or circuit thrombosis

  4. transfusions

    Time frame: through study completion, an average of 10 days

    Blood products transfusion requirements

Sponsors and collaborators

Lead sponsor

Policlinico Hospital

Other

Collaborators

  • The Mediterranean Institute for Transplantation and Advanced Specialized Therapies

Registry information

Official study title

Pilot Study of Antithrombin Supplementation During Extracorporeal Membrane Oxigenation

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Jul 5, 2017
Registry last updated
May 17, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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