Tenecteplase in Wake-up Ischaemic Stroke Trial

Status unconfirmed · Phase 3

Conditions studied: Ischemic Stroke, Stroke, Acute

In brief

Stroke is a leading causes of death and disability. At least 20% of strokes occur during sleep, so- called 'wake up stroke'. Thrombolysis with the clot-busting drug alteplase is effective for acute ischaemic stroke, provided that it is given within 4.5 hours of symptom onset. Patients with wake-up stroke are currently ineligible for clot-busting therapy. Previous studies indicate that many wake-up strokes occur just before awakening. In this study, patients with wake-up stroke will be randomized to thrombolysis with tenecteplase and best standard treatment or to best standard treatment without thrombolysis. Tenecteplase has several potential advantages over alteplase, including very rapid action and that it can be given as a single injection. Prior to thrombolysis, a brain scan must be done to exclude bleeding or significant brain damage as a result from the stroke. We will use a CT scan to inform this decision. CT is used as a routine examination in all stroke patients. Other studies testing clot-busting treatment in wake-up stroke are using alteplase and more complex brain scans, which are not routinely available in the emergency situation in all hospitals.

Key facts

Study ID

NCT03181360

Run by

University Hospital of North Norway

People needed

600

Starts

2017-06-12

Expected to finish

2022-12-31

Last updated by the study team

2021-05-14

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Stroke symptoms on awakening that were not present before sleep
• Clinical diagnosis of stroke with limb weakness with NIHSS score >=3, or dysphasia
• Treatment with tenecteplase is possible within 4.5 hours of awakening
• Written consent from the patient, non-written consent from the patient (witnessed by non-participating health care personnel), or written consent from the nearest family member

You may not qualify if…

• Age <18 years
• NIHSS score >25 or NIHSS consciousness score >2, or seizures during stroke onset
• Findings on plain CT that indicate that the patient is unlikely to benefit from treatment:
• Infarction comprising more than >1/3 of the middle cerebral artery territory on plain CT or CT perfusion
• Intracranial haemorrhage, structural brain lesions which can mimic stroke (e.g cerebral tumour)
• Active internal bleeding of high risk of bleeding, e.g.:
• Major surgery, trauma or gastrointestinal or urinary tract haemorrhage within the previous 21 days, or arterial puncture at a non-compressible site within the previous 7 days
• Any known defect in coagulation, e.g. current use of vitamin K antagonist with an INR >1.7 or prothrombin time >15 seconds, or use of direct thrombin inhibitors or direct factor Xa inhibitors during the last 24 hours (unless reversal of effect can be achieved by agents such as idarucizumab) or with elevated sensitive laboratory tests (such as activated partial thromboplastin time (aPTT), international normalized ratio (INR), platelet count, ecarin clotting time, thrombin time (TT), or appropriate factor Xa activity assays), or heparins during the last 24 hours or with an elevated aPTT greater than the upper limit of normal
• Known defect of clotting or platelet function or platelet count below 100,000/mm3 (but patients on antiplatelet agents can be included)
• Ischaemic stroke or myocardial infarction in previous 3 months, previous intracranial haemorrhage, severe traumatic brain injury or intracranial or intraspinal operation in previous 3 months, or known intracranial neoplasm, arteriovenous malformation or aneurysm
• Contraindications to tenecteplase, e.g., acute bacterial endocarditis or pericarditis; acute pancreatitis; severe hepatic dysfunction, including hepatic failure, cirrhosis, portal hypertension; active hepatitis; systemic cancer with increased bleeding risk; haemostatic defect including secondary to severe hepatic, renal disease; organ biopsy; prolonged cardiopulmonary resuscitation > 2 min (within 2 weeks)
• Persistent blood pressure elevation (systolic ≥185 mmHg or diastolic ≥110 mmHg), despite blood pressure lowering treatment
• Blood glucose <2.7 or >20.0 mmol/L (use of finger-stick measurement devices is acceptable)
• Pregnancy, positive pregnancy test, childbirth during last 10 days, or breastfeeding. In any woman of childbearing potential, a pregnancy test must be performed and the result assessed before trial entry
• Other serious or life-threatening disease before the stroke: severe mental or physical disability (e.g. Mini Mental Status score <20, or mRS score ≥3), or life expectancy less than 12 months
• Patient unavailability for follow-up (e.g. no fixed address)

Where it is running

• University Hospital of North Norway, Harstad — Harstad, Norway (enrolling)
• Sørlandet sykehus Kristiansand HF — Kristiansand, Norway (enrolling)
• Pärnu Hospital — Pärnu, Estonia (enrolling)
• Helse Finnmark Hammerfest — Hammerfest, Norway (enrolling)
• Odense University Hospital — Odense, Denmark (enrolling)
• Tartu University Clinic — Tartu, Estonia (enrolling)
• Satakunta Central Hospital — Pori, Satakunta, Finland (enrolling)
• Helsinki University Hospital — Helsinki, Finland (enrolling)
• East Tallin Central Hospital — Tallinn, Estonia (enrolling)
• Bispebjerg hospital — Copenhagen, Denmark (enrolling)
• Central Hospital in Vaasa — Vaasa, Finland (enrolling)
• West Tallin Central Hospital — Tallinn, Estonia (enrolling)
• Alytus S. Kudirkos Hospital — Alytus, Lithuania (enrolling)
• Lithuanian University of Health Sciences Kauno Klinikos — Kaunas, Lithuania (enrolling)
• Klaipeda Seamen's Hospital — Klaipėda, Lithuania (enrolling)
• Republican Vilnius University Hospital — Vilnius, Lithuania (enrolling)
• Vilnius University Hospital — Vilnius, Lithuania (enrolling)
• Christchurch Hospital — Christchurch, New Zealand (enrolling)
• Siun sote - Joint municipal authority for North Karelia social and health services — Joensuu, Finland (enrolling)
• Ålesund sjukehus Helse Møre og Romsdal — Ålesund, Norway (enrolling)
• Pohjois-Kymen sairaala — Kouvola, Finland (enrolling)
• Sørlandet Sykehus HF Flekkefjord — Flekkefjord, Norway (enrolling)
• Helse Førde HF — Førde, Norway (enrolling)
• Nordlandssykehuset Lofoten Gravdal — Gravdal, Norway (enrolling)
• Akershus universitetssykehus (Ahus) — Lørenskog, Norway (enrolling)

Full record on ClinicalTrials.gov

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