Randomization to Extend Stroke Intravenous ThromboLysis In Evolving Non-Large Vessel Occlusion With TNK (RESILIENT

Launched by HOSPITAL MOINHOS DE VENTO · Jan 5, 2022

Keywords

ClinConnect Summary

The RESILIENT trial is a research study aimed at finding out if a treatment called Tenecteplase (TNK) is more effective than a placebo (a substance with no active treatment) for patients who have suffered an ischemic stroke caused by a non-large vessel occlusion. This study is specifically looking at patients who are treated within 4.5 to 12 hours after their last normal health check. The goal is to help those who can't receive standard treatments due to the timing of their stroke and the type of blood vessel involved.

To be eligible for this trial, participants must be at least 18 years old, have suffered an acute ischemic stroke without significant prior disability, and have certain imaging results that show they might benefit from TNK treatment. Patients will be randomly assigned to receive either TNK or a placebo, and the trial is currently recruiting participants. It's important to note that if you or a loved one are considering this trial, you'll need to provide informed consent, which means you’ll be fully informed about the study and agree to participate. This research aims to improve treatment options for stroke patients, potentially leading to better recovery outcomes.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Acute ischemic stroke where patient is ineligible for IV thrombolytic treatment with Alteplase due to onset \>4.5 hours and is ineligible for endovascular treatment under standard of care due to absence of proximal arterial occlusion (e.g. intracranial ICA, MCA-M1 and dominant M2 segments, and vertebrobasilar arteries).
• • \* Dominant M2 segment is defined is a division supplying \>50% of the MCA territory vs co-dominant supplying 50% of the MCA territory vs non-dominant supplying \<50% of the MCA territory.
• • 2. No significant pre-stroke functional disability (mRS ≤2).
• • 3. Age ≥18 years (no upper age limit).
• 4. Clinical or imaging mismatch evidence in distal artery territories, defined as one of the following scenarios (A, B or C):
• * Scenario A - all of the following:
• • Significant cortical neurological deficit (moderate to severe afasia, moderate to severe heminegligence, severe hemianopsia) with the addition or not of motor symptoms OR any motor deficit accompanied of cortical symptoms of any severity;
• • Contrast-enhanced CT of the head or head MRI with \<50% involvement of the vascular territory corresponding to the clinical manifestation;
• • Arterial head angiotomography or arterial head angioMRI WITHOUT proximal intracranial artery occlusion that would require endovascular therapy (for example, ICA intracranial, MCA-M1 and M2 dominant segments and vertebral and basilar arteries)
• * Scenario B - all of the following:
• • NIHSS score ≥ 4 due to any neurologic deficits;
• • Non-contrast CT of the head or head MRI com \<50% involvement of the vascular territory corresponding to the clinical manifestation;
• • Arterial head angioCT or arterial head MRI WITHOUT proximal intracranial artery occlusion that would require endovascular therapy (for example, ICA intracranial, MCA-M1 and M2 dominant segments and vertebral and basilar arteries)
• • Arterial head angioCT with distal occlusion on MIP or wedge-shaped lesion on parenchymography on the source-image of angiotomography OR CT perfusion with wedge-shaped cortical lesion.
• * Scenario C - all of the following:
• • NIHSS score ≥ 4 due to any neurologic deficits;
• * The presence of a Target Mismatch defined as:
• • Ischemic Core \<50cc (defined on NCCT/CTP\* or DWI MRI) \*Volume NCCT can be used to exclude patients if the investigator believes that its volume assessment is more reliable that the CTP in any particular case.
• • Mismatch Volume (Tmax \>6sec lesion - Core volume lesion) \>10cc
• • Mismatch Ratio \>1.4
• • 5. Patient treatable within 4.5-12 hours of symptom onset. Symptoms onset is defined as point in time the patient was last seen well (at baseline). Treatment start is defined as initiation of IV TNK or placebo infusion.
• • Patients who have woken up with the symptoms and don't have a mismatch FLAIR-DWI according to the WAKE-UP Trial image criteria will have their window considered to be \>4.5 hours. In this case, the time last seen well must have been 12 hours at most.
• • 6. Informed consent obtained from patient or acceptable patient surrogate.
• Exclusion Criteria:
• • 1. Intracranial hemorrhage (ICH) identified by CT or MRI.
• • 2. Rapidly improving symptoms, particularly if in the judgment of the managing clinician that the improvement is likely to result in the patient without eligibility criteria.
• • 3. Pre-stroke mRS score of ≥ 2 (indicating previous disability)
• • 4. Contra indication to imaging with MR or CT with contrast agents.
• • 5. Infarct core \>1/3 MCA territory qualitatively or \>50 mL quantitatively (determined by DWI lesion on MR).
• • 6. Participation in any investigational study in the previous 30 days
• • 7. Any terminal illness such that patient would not be expected to survive more than 1 year).
• • 8. Baseline platelet count \< 100.000/µL
• • 9. Woman of childbearing potential who is known to be pregnant or who has a positive pregnancy test on admission.
• • 10. Previous stroke within last three months.
• • 11. Recent past history or clinical presentation of ICH, subarachnoid hemorrhage (SAH), arterio-venous (AV) malformation, aneurysm, or cerebral neoplasm other than meningioma.
• • 12. Current use of oral anticoagulants and a prolonged prothrombin time (INR \> 1.6).
• • 13. Use of heparin, except for low dose subcutaneous heparin, in the previous 48 hours and a prolonged partial thromboplastin time exceeding the upper limit of the local laboratory normal range
• • 14. Use of glycoprotein IIb - IIIa inhibitors within the past 72 hours. Use of single agent oral platelet inhibitors (clopidogrel or low-dose aspirin) prior to study entry is permitted.
• • 15. Clinically significant hypoglycemia.
• • 16. Uncontrolled hypertension defined by a blood pressure \> 185 mmHg systolic or \>110 mmHg diastolic on at least 2 separate occasions at least 10 minutes apart, or requiring aggressive treatment to reduce the blood pressure to within these limits. The definition of "aggressive treatment" is left to the discretion of the responsible Investigator.
• • 17. Hereditary or acquired hemorrhagic diathesis.
• • 18. Gastrointestinal or urinary bleeding within the preceding 21 days.
• • 19. Major surgery within the preceding 14 days which poses risk in the opinion of the Investigator.
• • 20. Exposure to a thrombolytic agent within the previous 72 hours.
• • 21. Subject participating in a study involving an investigational drug or device that would impact this study.