Phase
Condition
Stroke
Thrombosis
Cerebral Ischemia
Treatment
Tenecteplase
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria
Informed consent
Age ≥18 years
Clinical signs consistent with an acute ischemic stroke
Patient had an initial vessel occlusion in the anterior or posterior circulation defined as intracranial ICA, M1, M2, M3, A1, A2, P1 or P2
Patient has undergone endovascular stroke treatment
Onset to randomization no later than < 705 minutes (11h 45min) after symptom-onset/last-seen well.
Incomplete reperfusion defined as any of the following:
For ICA/M1: TICI2b/2c (50-99%) reperfusion after endovascular treatment without mechanically amendable target-occlusion (as per definition by the interventionalist).
For A1/A2, P1/P2, M2/M3: TICI2a/2b/2c (1-99%) reperfusion after endovascular treatment without mechanically amendable target-occlusion (as per definition by the interventionalist).
Any emboli to new territory without mechanically amendable target-occlusion (as per definition by the interventionalist).
- Signs of early ischemic changes of non-contrast CT Alberta Stroke Program Early CT Score (ASPECTS) ≥5 (for DWI-ASPECTS ≥ 4, for DWI-ASECTS: a region must have diffusion abnormality in 20% or more of its volume to be considered DWI-ASPECTS positive)
Exclusion Criteria
Acute intracranial hemorrhage
Contraindication to MRI (e.g. pacemaker)
Any severe bleeding within the past 6 months, which would prevent administration of intravenous thrombolysis in clinical routine Major surgery in the past 2 months with severe risk of bleeding, which would prevent administration of intravenous thrombolysis in clinical routine
Intake of Vitamin K antagonists with INR >1.7
Platelets < 50,000
Non-controlled hypertension (defined as SBP >185 mmHg or DBP >110 mmHg refractory to treatment)
Active dyspeptic ulcer
Known arterial aneurysm
Known neoplasms with risk of bleeding
Severe liver fibrosis or portal hypertension
Acute pericarditis
Acute endocarditis
Acute pancreatitis
Known allergy to TNK or Gentamicin or other additives/auxiliaries (Polysorbatum 20, L-Argininum, Acidum phosphoricum)
Known Renal failure either as defined by a serum creatinine > 3.0 mg/dl (or 265.2 μmol/l) or glomerular Filtration Rate [GFR] < 30 or as subject who required hemodialysis/peritoneal dialysis
Radiological confirmed evidence of mass effect or intracranial tumor (except small meningioma)
Radiological confirmed evidence of cerebral vasculitis
Calcified thrombi
Pregnancy or lactating women
Study Design
Connect with a study center
LKH-Universitätsklinikum Graz
Graz, 8036
AustriaSite Not Available
Medizinische Universität Innsbruck
Innsbruck, 6020
AustriaSite Not Available
Kepler Universitätsklinikum GmbH
Linz, 4020
AustriaSite Not Available
Christian-Doppler-Klinik Salzburg
Salzburg, 5020
AustriaActive - Recruiting
Hôpital universitaires de Bruxelles
Anderlecht, 1070
BelgiumActive - Recruiting
AZ Sint Jan Brugge AV
Brugge, 8000
BelgiumSite Not Available
UZ Brussel
Brussel, 1050
BelgiumSite Not Available
Cliniques universitaires Saint-Luc
Bruxelles, 1200
BelgiumActive - Recruiting
UZA Antwerpen
Edegem, 2650
BelgiumSite Not Available
Universitair Ziekenhuis Gent
Gent, 9000
BelgiumSite Not Available
UZ Gasthuisberg Leuven
Leuven, 3000
BelgiumActive - Recruiting
Clinique CHC MontLégia
Liège, 4000
BelgiumActive - Recruiting
University Hospital Helsinki
Helsinki, 00029
FinlandActive - Recruiting
Universitätsklinikum Augsburg
Augsburg, 86156
GermanyActive - Recruiting
Universitätsklinikum Bonn
Bonn, 53127
GermanyActive - Recruiting
Klinikum Bremen-Mitte
Bremen, 28205
GermanySite Not Available
Universitätsklinikum Carl Gustav Carus an der Technischen Universität Dresden
Dresden, 01307
GermanyActive - Recruiting
Helios Klinikum Erfurt
Erfurt, 99089
GermanySite Not Available
Universitätsklinikum Frankfurt
Frankfurt, 60528
GermanyActive - Recruiting
Universitätsklinikum Freiburg
Freiburg, 79106
GermanyActive - Recruiting
Universitätsmedizin Göttingen
Göttingen, 37075
GermanyActive - Recruiting
Universitätsklinikum Halle (Saale)
Halle, 06120
GermanyActive - Recruiting
Asklepios Klinik Altona
Hamburg, 22763
GermanyActive - Recruiting
Universitätsklinikum Hamburg-Eppendorf
Hamburg, 20246
GermanyActive - Recruiting
Universitätsklinikum Schleswig-Holstein Campus Kiel
Kiel, 24105
GermanyActive - Recruiting
Universitätsklinikum Magdeburg A. ö. R.
Magdeburg, 39120
GermanyActive - Recruiting
Universitätsmedizin Mannheim
Mannheim, 68167
GermanyActive - Recruiting
Johannes Wesling Klinikum Minden
Minden, 32429
GermanySite Not Available
Klinikum der Universität München
München, 81377
GermanySite Not Available
Klinikum rechts der Isar der Technischen Universität München
München, 81675
GermanySite Not Available
Universitätsklinikum Münster
Münster, 48149
GermanySite Not Available
Universitätsklinikum Tübingen
Tübingen, 72076
GermanyActive - Recruiting
Universitätsspital Basel
Basel,
SwitzerlandActive - Recruiting
Universitätsspital Bern
Bern, 3010
SwitzerlandActive - Recruiting
Hôpitaux universitaires de Genève
Genève, 1211
SwitzerlandActive - Recruiting
Ospedale Regionale di Lugano
Lugano, 6900
SwitzerlandActive - Recruiting
Kantonsspital Luzern
Luzern, 6000
SwitzerlandActive - Recruiting
Kantonsspital St.Gallen
St.Gallen, 9007
SwitzerlandActive - Recruiting
Universitätsspital Zürich
Zürich, 8091
SwitzerlandActive - Recruiting
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