Mode
Text Size
Log in / Sign up
N/A Completed N=328 Treatment

The Imperative Trial: Treatment of Acute Ischemic Stroke With the Zoom Reperfusion System

Source: ClinicalTrials.gov NCT04129125 ↗
Enrolled (actual)
328
Serious AEs
36.5%
Results posted
Aug 2025
Primary outcomePrimary: ITT Cohort: Rate of Core Lab-adjudicated Reperfusion Success — 216 Participants — p=<0.0001

Summary

The trial is designed to assess the safety and efficacy of using the Zoom Reperfusion System in subjects diagnosed with acute ischemic stroke and undergoing a thrombectomy procedure within 8 hours of last known well.

Outcome Measures

OutcomeResultp-value
PRIMARY
ITT Cohort: Rate of Core Lab-adjudicated Reperfusion Success
216 <0.0001 sig
PRIMARY
ITT Cohort: Rate of Symptomatic Intracranial Hemorrhage (sICH), as Independently Adjudicated by Core Lab and Safety Board
5 —
PRIMARY
FDA Clearance Cohort: Rate of Core Lab-adjudicated Reperfusion Success
177 0.0001 sig
PRIMARY
FDA Clearance Cohort: Rate of Symptomatic Intracranial Hemorrhage (sICH), as Independently Adjudicated by Core Lab and Safety Board
2 —
PRIMARY
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of Core Lab-adjudicated Reperfusion Success
125 —
PRIMARY
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of Symptomatic Intracranial Hemorrhage (sICH), as Independently Adjudicated by Core Lab and Safety Board
1 —
SECONDARY
ITT Cohort: Time to Achieve mTICI Score ≥ 2b
19 —
SECONDARY
ITT Cohort: Rate of mTICI Score 3 Reperfusion
78 —
SECONDARY
ITT Cohort: Rate of First Pass Success
148 —
SECONDARY
ITT Cohort: Rate of mTICI Score 2c Reperfusion
147 —
SECONDARY
ITT Cohort: Rate of Functional Independence
133 —
SECONDARY
ITT Cohort: Quality of Life Assessment
71.5; 71; 79.9; 78.9; 85; 76.3 —
SECONDARY
ITT Cohort: Rate of All-Cause Mortality
33 —
SECONDARY
ITT Cohort: Rate of All Intracranial Hemorrhage (ICH)
53 —
SECONDARY
ITT Cohort: Rate of Embolization in New Territory (ENT)
2 —
SECONDARY
ITT Cohort: Rate of Serious Adverse Device Effects (SADEs)
5 —
SECONDARY
ITT Cohort: Rate of Serious Adverse Events
95 —
SECONDARY
FDA Clearance Cohort: Time to Achieve mTICI Score ≥ 2b
19 —
SECONDARY
FDA Clearance Cohort: Rate of mTICI Score 3 Reperfusion
65 —
SECONDARY
FDA Clearance Cohort: Rate of First Pass Success
128 —
SECONDARY
FDA Clearance Cohort: Rate of mTICI Score 2c Reperfusion
124 —
SECONDARY
FDA Clearance Cohort: Rate of Functional Independence
110 —
SECONDARY
FDA Clearance Cohort: Quality of Life Assessment
72.7; 72.4; 79.8; 79.2; 85.7; 77.8 —
SECONDARY
FDA Clearance Cohort: Rate of All-Cause Mortality
26 —
SECONDARY
FDA Clearance Cohort: Rate of All Intracranial Hemorrhage (ICH)
42 —
SECONDARY
FDA Clearance Cohort: Rate of Embolization in New Territory (ENT)
2 —
SECONDARY
FDA Clearance Cohort: Rate of Serious Adverse Device Effects (SADEs)
3 —
SECONDARY
FDA Clearance Cohort: Rate of Serious Adverse Events
74 —
SECONDARY
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Time to Achieve mTICI Score ≥ 2b
18 —
SECONDARY
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of mTICI Score 3 Reperfusion
46 —
SECONDARY
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of First Pass Success
87 —
SECONDARY
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of mTICI Score 2c Reperfusion
84 —
SECONDARY
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of Functional Independence
67 —
SECONDARY
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Quality of Life Assessment
69; 69.4; 76.5; 78.6; 84.7; 74.6 —
SECONDARY
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of All-Cause Mortality
21 —
SECONDARY
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of All Intracranial Hemorrhage (ICH)
29 —
SECONDARY
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of Embolization in New Territory (ENT)
2 —
SECONDARY
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of Serious Adverse Device Effects (SADEs)
3 —
SECONDARY
FDA Clearance Cohort for Distal ICA/M1 Occlusions: Rate of Serious Adverse Events
54 —

Eligibility Criteria

Inclusion Criteria

  • Age 18 and older
  • NIHSS >=6
  • The operator feels that the stroke can be treated with endovascular thrombectomy approaches and the interventionalist estimates that groin puncture can be achieved within 8 hours from time last seen well
  • Pre-event mRS scale 0-1
  • Large vessel occlusion of the intracranial internal carotid artery (ICA), middle cerebral artery (MCA)-M1 or M2 segments, basilar, or vertebral arteries as evidenced by MRA or CTA
  • For strokes in anterior circulation, ASPECTS >=6; For strokes in posterior circulation, pc-ASPECTS >=8
  • Non-contrast CT/CTA or MRI/MRA for trial eligibility performed or repeated at treating stroke center or outside medical facility within 2 hours of treatment initiation
  • If indicated per American Heart Association clinical guidelines, thrombolytic therapy should be administered as soon as possible
  • Consenting requirements met according to local IRB or Ethics Committee

Exclusion Criteria

  • Female known to be pregnant at time of admission
  • Patient has suffered a stroke in the past 3 months
  • Presence of an existing or pre-existing large territory infarction
  • Pre-existing neurological or psychiatric disease that would confound the neurological or functional evaluation, e.g., dementia with prescribed anti-cholinesterase inhibitor
  • Known history of severe contrast allergy or absolute contraindication to iodinated contrast
  • Clinical history, past imaging or clinical judgement suggest that the intracranial occlusion is chronic
  • Life expectancy of less than 6 months prior to stroke onset
  • Clinical symptoms suggestive of bilateral stroke or stroke in multiple territories
  • Subject participating in another clinical trial involving an investigational device or drug
  • Known cancer with metastases
  • Evidence of active systemic infection
  • Any known hemorrhagic or coagulation deficiency

Imaging Exclusion Criteria:

  • Evidence of intracranial hemorrhage on CT/MRI
  • CTA or MRA evidence of carotid stenosis requiring treatment for intracranial access
  • Excessive vascular access tortuosity or target vessel size that will likely prevent endovascular access with the Imperative Care 0.088" ID Catheters
  • Intracranial stent implanted in the same vascular territory that would preclude the safe deployment/removal of the thrombectomy devices
  • Occlusions in multiple vascular territories (e.g., bilateral anterior circulation, or anterior circulation/vertebrobasilar system) as confirmed on CTA/MRA, or clinical evidence of bilateral strokes or strokes in multiple territories as determined by the treating physician
  • Significant mass effect with midline shift as confirmed on CT/MRI
  • Evidence of intracranial tumor (except small meningioma defined as ≤ 3cm and asymptomatic) as confirmed on CT/MRI
  • Angiographic evidence of pre-existing arterial injury, e.g., carotid dissection, complete cervical carotid occlusion, or vasculitis
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04129125). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

Back to search