Skip to main content
Clinical Trials/NCT02902393
NCT02902393
Unknown
Not Applicable

Interest of Thromboelastography (ROTEM) as a Biomarker of Revascularisation in Stroke

University Hospital, Caen1 site in 1 country64 target enrollmentJuly 2016
ConditionsStroke

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke
Sponsor
University Hospital, Caen
Enrollment
64
Locations
1
Primary Endpoint
Evaluation of revascularisation 24 hours after tPA injection using CT scan or MRI
Last Updated
9 years ago

Overview

Brief Summary

Revascularisation using recombinant tPA is the reference treatment of stroke. However, the efficacy of fibrinolysis is about 50%. Several factors, including the size of thrombus, have been associated with revascularisation efficacy.

The aim of this prospective study is to evaluate ex vivo the effect of tPA in patients with stroke with thromboelastography and to correlate results with the clinical outcome of patients. Results may predict revascularisation in patients with stroke.

Registry
clinicaltrials.gov
Start Date
July 2016
End Date
September 2018
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patient (\> 18 years) with a neurological deficit compatible with a neurovascular pathology eligible for fibrinolysis rtPA and having a proximal occlusion of the middle cerebral artery (segment M1 / M2) or basilar trunk objectified brain imaging (MRI angiography or angio CT).

Exclusion Criteria

  • Any patient with major comorbidity, a pathology of hemostasis or anticoagulant treatment (vitamin K antagonist (VKA), direct oral anticoagulant).

Outcomes

Primary Outcomes

Evaluation of revascularisation 24 hours after tPA injection using CT scan or MRI

Time Frame: 24 hours

Secondary Outcomes

  • Clinical evaluation using NIHSS scale(24 hours)

Study Sites (1)

Loading locations...

Similar Trials