Alteplase-Tenecteplase Trial Evaluation for Stroke Thrombolysis- (ATTEST)

Stroke Clinical Trial

— ATTEST  

Official title:

Alteplase-Tenecteplase Trial Evaluation for Stroke Thrombolysis - Pilot Phase (ATTEST)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01472926
• Other study ID #: 2010-024541-67
• Secondary ID: TSA 2010/042010-
• Status: Completed
• Phase: Phase 2
• Start date: December 2011
• Est. completion date: December 10, 2013

Study information

• Verified date: August 2012
• Source: NHS Greater Glasgow and Clyde
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A pilot evaluation of tenecteplase compared to alteplase in acute ischaemic stroke patients currently eligible for intravenous alteplase treatment in a prospective, randomised, blinded outcome evaluation clinical trial using brain imaging as a biomarker.

Description:

Newer thrombolytic agents such as tenecteplase have pharmacological features (higher fibrin binding specificity and longer half-life) that may be advantageous when compared to older agents such as alteplase with respect to arterial recanalisation, ease of administration, and reduced bleeding risk. No other clinical trial is currently evaluating alternative thrombolytic strategies in patients who are eligible to receive standard intravenous alteplase, instead concentrating on extending the population for IV thrombolysis.

The ATTEST pilot phase will use brain imaging as a biomarker for key clinical response variables, with penumbral salvage as the primary end-point and secondary end-points including recanalisation as well as conventional clinical scales.

The findings of this study are anticipated to provide data on sample size and event rates to inform the design of a definitive, confirmatory, pragmatic, randomised, controlled trial with clinical endpoints.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 104
• Est. completion date: December 10, 2013
• Est. primary completion date: December 10, 2013
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• clinical diagnosis of supratentorial acute ischaemic stroke with score of at least 1 on the NIH Stroke Scale

• male or non pregnant female >=18 years

• within 4.5 hours of onset as defined by time since last known well

• CT perfusion and CT Angiogram examination acquired prior to treatment

Exclusion Criteria:

• Contraindications to thrombolytic drug treatment for stroke

• Evidence of intracranial haemorrhage or significant non-stroke intracranial pathology (including central nervous system neoplasm, aneurysm or arteriovenous malformation) on pre-treatment CT

• Established hypodensity on pre-treatment brain CT of more than one third of the middle cerebral artery territory or Alberta Stroke Programme Early CT (ASPECT) Score <4 (sulcal effacement or loss of grey-white differentiation in cortical territories alone are not counted towards ASPECT score)

• Hypodensity consistent with recent cerebral ischaemia other than the presenting event

• Very severe stroke (eg NIHSS>25)

• systolic blood pressure (BP)> 185 or diastolic BP> 110 mm Hg, or aggressive management (intravenous pharmacotherapy) necessary to reduce BP to these limits

• If on warfarin, International Normalised Ratio (INR) <1.4

• Current prescription of non-warfarin oral anticoagulant drugs

• Significant abnormality of coagulation parameters pre-treatment (prolonged INR or activated partial thromboplastin time (APTT), or platelet count <100,000/mm3)

• administration of heparin within the previous 48 hours and a thromboplastin time exceeding the upper limit of normal for laboratory, or use of therapeutic dose low molecular weight heparin within 48h

• Clinical history suggestive of subarachnoid haemorrhage even if no blood is evident on CT

• Risk of bleeding (Major surgery within previous 1 month; intracranial or spinal surgery; recent trauma to the head or cranium; prolonged cardiopulmonary resuscitation (> 2 minutes) within the past 2 weeks; acute pericarditis and/or subacute bacterial endocarditis; acute pancreatitis; severe hepatic dysfunction, including hepatic failure, cirrhosis, portal hypertension (oesophageal varices) and active hepatitis; active peptic ulceration; any known history of haemorrhagic stroke or stroke of unknown origin; arterial aneurysm and known arteriovenous malformation)

• Dependent (mRS 3-5) pre-stroke

• Blood glucose <2 mmol/l or >18 mmol/l

• Seizure at onset of symptoms unless brain imaging identifies positive evidence of significant brain ischaemia (eg CTA confirmed arterial occlusion, early ischaemic change on plain CT, hypoperfusion on CTP)

• Pregnancy

• Known impaired renal function (estimated Glomerular Filtration Rate <30 ml/min) precluding contrast CT

• Known allergy to radiological contrast

• History of allergies to active substances in either trial medication, or to excipients including gentamicin

• Severe concurrent medical condition that would prevent participation in study procedures (e.g. cardia failure with severe pulmonary oedema)or with life expectancy <=3 months

Related Conditions & MeSH terms

• Stroke

Intervention

Drug:
• Tenecteplase
Intravenous (IV) tenecteplase 0.25 mg/kg (single bolus; maximum dose 25 mg)
• alteplase
Intravenous alteplase 0.9mg/kg to maximum of 90mg, given as 10% bolus and 90% of dose over 1 hour infusion

Locations

Country	Name	City	State
United Kingdom	Southern General Hospital	Glasgow	Scotland

Sponsors (2)

Lead Sponsor	Collaborator
NHS Greater Glasgow and Clyde	University of Glasgow

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Percent penumbral salvage at 24-48h (initial penumbra volume on computed tomography perfusion (CTP) imaging versus 24-48h CT infarct volume.	Percent penumbral salvage at 24-48h (initial CTP-defined penumbra volume versus 24-48h CT infarct volume.	48 hours
Secondary	Proportion of patients exhibiting recanalisation (on computed tomography angiography, CTA) 24-48 hours post treatment	Proportion of patients exhibiting recanalisation (measured by CTA) 24-48 hours post treatment	48 hours
Secondary	Early clinical improvement 24 hours post treatment	Early clinical improvement (National Institutes of Health Stroke Scale [NIHSS] score reduced by >=4 points, or = 0 or 1) 24 hours post treatment	24 hours
Secondary	Proportion of patients with symptomatic intracerebral haemorrhage (SICH) on 24-48 hour CT	Proportion of patients with symptomatic ICH (SICH) on 24-48 hour CT: by Safe Implementation of Thrombolysis Monitoring Study (SITS-MOST) definition - parenchymal haematoma type 2 (PH2/PHr2) + NIHSS deterioration by >=4 points at 24 hours; Any ICH	48 hours
Secondary	Distribution of functional outcome by modified Rankin Scale (mRS) scores at Day 30	Distribution of outcome scores on the modified Rankin Scale (mRS)	30 Days
Secondary	Distribution of functional outcome scores (mRS) at Day 90	Distribution of functional outcome scores (mRS)	90 days
Secondary	Proportion of patients with favourable clinical outcome (mRS 0-1) at Day 30	Proportion of patients with favourable clinical outcome (mRS 0-1)	30 days
Secondary	Proportion of patients with favourable clinical outcome (mRS 0-1) at Day 90	Proportion of patients with favourable clinical outcome (mRS 0-1)	90 days
Secondary	Average 'home time' by day 90	Average 'home time' (number of nights spent in non-institutional private residence) by Day 90	90 Days
Secondary	Mortality at Day 90		90 Days