Treatment of Acute Ischemic Stroke With CATCHVIEW Stent Retriever in Comparison to SOLITAIRE 2/FR

Withdrawn

• Conditions: Acute Ischemic Stroke
• Interventions: Device: CATCHVIEW

• Registration Number: NCT03754296
• Lead Sponsor: Balt Extrusion

Brief Summary

The TRUST study is a non-interventional, prospective, multicenter, international, single arm and non-inferiority study. It is designed to evaluate the efficacy and safety of mechanical thrombectomy of the CATCHVIEW device compared to SOLITAIRE 2/FR based on an objective performance criterion (OPC) defined with available and published clinical evidence gathered through the Solitaire clinical trials in the arterial revascularization of patients with acute ischemic stroke.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2018-11-23
• Study First Submitted QC: 2018-11-23
• Study First Posted: 2018-11-27
• Study Start: 2018-12
• Status Verified: 2020-01
• Last Update Submitted: 2020-01-06
• Last Update Posted: 2020-01-09
• Primary Completion: 2020-03
• Study Completion: 2020-03

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• Age ≥ 18 and ≤ 80 years old
• Clinical signs consistent with acute ischemic stroke
• Pre-stroke modified Rankin Score ≤ 1
• Patient able to be treated within 8 hours of onset of stroke symptoms and within 2 hours between qualifying imaging from CTA or MRA to groin puncture
• Initial NIHSS ≥ 6 and < 30 at the time of inclusion
• Arterial occlusion in the intracranial internal carotid, M1/M2 segment of the MCA, carotid terminus or tandem proximal ICA/MCA-M1 confirmed by CT or MR angiography that is accessible to the device
• Acute ischemic stroke where patient is ineligible for IV thrombolytic treatment or the treatment is contraindicated (e.g., patient presents beyond recommended time from symptom onset), or where patient has received IV thrombolytic therapy without partial or complete recanalization
• Primary use of the CATCHVIEW stent retriever for the procedure (decision of use is done independently and prior to the participation of the patient in the study)
• Life expectancy of at least 90 days
• Ability of the patient or legally authorized representative to provide a signed and dated informed consent form before the procedure. Where applicable, in case of medical emergency not allowing the patient to provide consent and unavailability of the legally authorized representative, a physician who does not take part in the study will sign the informed consent before the procedure. In any case, the patient or the legally authorized representative consent shall be requested as soon as possible after the procedure up until the discharge visit.

Exclusion Criteria

Clinical exclusion criteria

• Clinical presentation suggests a subarachnoid hemorrhage, even if initial CT or MRI scan is normal
• Suspicion of aortic dissection
• Patient with a co-morbid disease or condition that would confound the neurological and functional evaluations or compromise survival or ability to complete follow-up assessments within 90 days
• Known history of other arterial disease that would prevent the device from reaching the target vessel and/or preclude safe recovery of the device
• Patient who requires hemodialysis or peritoneal dialysis, or who have contraindication to an angiogram for whatever reason
• Serious sensitivity to radiographic contrast agents
• Sensitivity to nickel-titanium
• Patient with stenosis proximal to the thrombus site that may preclude safe recovery of the device
• Inability to reach the occlusion site
• Known hemorrhagic diathesis, coagulation factor deficiency, or oral anticoagulant therapy with INR>3.0
• Current participation in an interventional investigation drug or device treatment study
• Pregnant women

Imaging exclusion criteria

• Baseline non-contrast CT or DWI MRI evidence of a moderate/large core defined as extensive early ischemic changes of Alberta Stroke Program Early CT score (ASPECTS) < 6
• Imaging evidence that suggests, in the opinion of the Investigator, the patient is not appropriate for mechanical thrombectomy intervention (e.g. inability to navigate to target lesion, moderate/large infarct with poor collateral circulation, etc.)
• CT or MRI evidence of hemorrhage on presentation
• CT or MRI evidence of mass effect or intra-cranial tumour (except small meningioma)
• Imaging evidence of cerebral vasculitis
• CT or MRI showing an infarction core involving greater than 1/3 of the MCA territory (or in other territories > 100 cc of tissue) on presentation
• CT or MRI evidence of a basilar artery (BA) occlusion or posterior cerebral artery (PCA) occlusion

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
CATCHVIEW stent retriever	CATCHVIEW	-

Primary Outcome Measures

Name	Time	Method
modified Rankin Score (mRS)	90 days	Proportion of patients achieving functional independence (mRS ≤ 2)