Clinical Trials Directory

Trials / Terminated

TerminatedNCT02839434

Evaluation of the Interference of Antithrombotic Agents With Laboratory Monitoring of Heparin Therapy

Status
Terminated
Phase
Study type
Observational
Enrollment
105 (actual)
Sponsor
Fondation Ophtalmologique Adolphe de Rothschild · Network
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Oral anticoagulants are increasingly prescribed and the are not discontinued for invasive cardiac procedures . Additional parenteral anticoagulation is necessary for these procedures (FA ablation and invasive coronary explorations). The unfractionated heparin doses are adapted on a monitoring test heparin, activated clotting time (ACT) with the aim of obtaining and maintaining an ACT \> 300-400 sec. This goal is the same whether the patient is on oral anticoagulant treatment or not, and regardless of the initial level of anticoagulation. The effects of oral anticoagulants on routine coagulation tests (PT, APTT, TT) are well documented, but few data have been published on the effects of heparin monitoring tests, particularly on the ACT. The aim of this stuy is to redefine the target values of ACT and unfractionated heparin doses to administer to optimize the efficacy / safety of invasive procedures in cardiology.

Conditions

Interventions

TypeNameDescription
PROCEDUREBlood sampleThis blood sample does not require specific puncture because it is made on the occasion of a sample justified by the patient monitoring.

Timeline

Start date
2015-12-01
Primary completion
2018-06-29
Completion
2018-06-29
First posted
2016-07-21
Last updated
2018-09-18

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT02839434. Inclusion in this directory is not an endorsement.