Clinical Trials Directory

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UnknownNCT03261284

D-dimer to Improve Anticoagulation Outcome During ECMO loNg-term supporteD

D-dimer to Improve Anticoagulation Management in Adult Patients Supported With Extracorporeal Membrane Oxygenation: a Prospective Cohort Study

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
300 (estimated)
Sponsor
Wuhan Asia Heart Hospital · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This was a prospective, cohort study.

Detailed description

Adult Patients receiving ECMO surpport in Wuhan Asia Heart Hospital were enrolled by cohort. Unfractionated heparin was used for Anticoagulation therapy, APTT or Anti-Xa activity is monitored for dose adjustment. Meanwhile, D-dimer is mornitored. If D-dimer levels continue to rise (\>1.5 times previous result ), increase the dose of heparin to reach the upper limit of the treatment target; If the D-dimer levels is stable (\<1.5 times previous result ) or is decreasing, the anticoagulation dose is maintained at current level (no active bleeding) or decreased (active bleeding). All patients were followed up The occurrence of endpoints during in-hospital and 30 days after discharge, including bleeding events, thrombotic events and all-cause deaths were recorded.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTD-dimer-guided adjustment strategeD-dimer-guided adjustment stratege
DIAGNOSTIC_TESTThepeautic-heparin therapy0.3-0.7U/ml of anti-Xa activity or APTT 1.5-2.5 times of control

Timeline

Start date
2019-03-01
Primary completion
2023-12-01
Completion
2023-12-30
First posted
2017-08-24
Last updated
2023-04-18

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03261284. Inclusion in this directory is not an endorsement.