Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07302620

HEPARINS: INTERFERENCE IN ARGATROBAN MEASUREMENT

Status
Recruiting
Phase
Study type
Observational
Enrollment
70 (estimated)
Sponsor
University Hospital, Strasbourg, France · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Unfractionated heparin (UFH) and low molecular weight heparins (LMWH) provide anticoagulation through their anti-Xa and anti-IIa activity. This anti-IIa activity can lead to an overestimation of argatroban's activity when switching to an anti-IIa anticoagulant such as argatroban. This situation can be critical because argatroban is generally administered following heparin therapy due to suspected heparin-induced thrombocytopenia. Therefore, there is both a significant thrombotic risk induced by the underlying condition and a hemorrhagic risk induced by the anticoagulation. For this reason, it is important to be able to accurately monitor the anti-IIa activity of argatroban. To date, the test used to determine the anti-IIa activity of argatroban at the Hematology Laboratory of the Strasbourg University Hospitals (HUS) is a modified thrombin time (with a calibration curve adapted for argatroban). When switching between several molecules with anti-IIa activity, this test does not allow for the differentiation of the anti-IIa activity attributable to each anticoagulant. There are no data in the literature to determine whether heparins interfere with this test, and if so, its extent.

Conditions

Timeline

Start date
2024-12-03
Primary completion
2026-01-01
Completion
2026-01-01
First posted
2025-12-24
Last updated
2025-12-24

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT07302620. Inclusion in this directory is not an endorsement.