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Study identifier: NCT06222866 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Anticoagulation and Inflammation Monitoring in Patients After Heart and Vascular Interventions

Condition: Heart Surgery · Vascular Surgery · Delirium  ·  Sponsor: Medical University Innsbruck

PhaseN/A
Planned participants400
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this prospective observational study is to evaluate the most appropriate anticoagulation monitoring tool for unfractionated heparin (UFH), by comparison of different monitoring modalities in relation to adverse events occurrence (thrombosis/bleeding). The main study questions are: * What is the most appropriate anticoagulation monitoring tool (ACT, aPTT, viscoelastic tests (ROTEM), and anti-Xa) for UFH * What is the incidence of adverse events associated with anticoagulation and inflammation after heart and vascular interventions * Is there an association of available anticoagulation thresholds and monitoring tests with bleeding and/or thrombosis occurrence * Is there an association of inflammation with delirium Secondary study objectives include: * Association of anticoagulation levels as measured by ACT, aPTT, viscoelastic tests (ROTEM), and anti-factor-Xa with adverse events * Correlation of each anticoagulation monitoring test with the UFH anti-Xa measurement * Correlation of each anticoagulation monitoring test with another (ACT, aPTT, ROTEM, anti-F-Xa) and the amount of blood loss post surgery * The incidence of UFH-rebound effect and the need for protamine application * Association of inflammation and increased / reduced need for anticoagulation titration * Correlation of anticoagulation dosing with anticoagulation monitoring tests and adverse events * The association of inflammation with adverse events * The association and impact of inflammation on me…

This description comes directly from the study's public registry record.

Talk to the study team

Sasa Rajsic, MD, PhD  ·  004367763004447  ·  sasa.rajsic@tirol-kliniken.at

Always discuss trial participation with your own doctor first.

Locations (1)

Medical University InnsbruckInnsbruck, Tyrol, AustriaRecruiting

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Source record: clinicaltrials.gov/study/NCT06222866