Gravity Stroke System for Recanalization of Large Vessel Occlusion Strokes

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorGravity Medical Technology, INC

About this trial

Supernova and Neutron are endovascular mechanical revascularization devices indicated to restore blood flow by removing thrombus from a large intracranial vessel in patients experiencing an acute ischemic stroke within 24 hours of symptom onset or from last known well time.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Subject has experienced an Acute Ischemic Stroke due to large intracranial vessel occlusion in at least one of the following intracranial vessels: internal carotid artery (ICA), M1and M2 segments of the middle cerebral artery (MCA), basilar, and vertebral artery.

Subject has been or will be treated with Supernova and/or Neutron devices as the initial device used to remove the thrombus

Subject is willing to participate in a 90-day follow-up visit.

Disqualifiers

Concurrent participation in another mechanical neurothrombectomy device trial or any other clinical trial with an active treatment arm where the study procedure or treatment might confound the results of the registry.

Trial design

Design model

Single group

Treatments tested in this trial

  • Supernova revascularization device

    Device

    Mechanical Thrombectomy

Treatment groups

3,000 Participants
are divided into 1 treatment group
Group A: Supernova revascularization deviceExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Successful reperfusion

Rate of successful reperfusion, defined as modified Thrombolysis in Cerebral Ischemia (mTICI) grade of 2b or higher Grade 0: No reperfusion Grade 3: Complete reperfusion

Time frame
Day 0 (end of procedure)
2

Symptomatic intracranial hemorrhage

Safety (Rate of symptomatic intracranial hemorrhage (sICH) as measured by the SITS-MOST criteria) The SITS-MOST definition of SICH is a local or remote type II parenchymal haemorrhage within 22 to 36 hours after treatment (or sooner) associated with a ≥ fourpoint deterioration on the NIHSS score from baseline or from the lowest score from baseline to 24 hours, or leading to death.

Time frame
sICH measured within 24 (18-36) hours of the procedure
3

All-cause mortality

Safety (All-cause mortality)

Time frame
All-cause mortality measured at 90 (±14) days

Secondary outcomes

1

Percentage of participants with a modified Rankin Scale (mRS) score of ≤2

Effectiveness (The modified Rankin Scale (mRS) is a commonly used scale for measuring the degree of disability or dependence in the daily activities of people who have suffered a stroke or other causes of neurological disability. The scale runs from 0-6 with "0" being perfect health without symptoms to "6" being death. Score 0: No symptoms Score 1: No significant disability. Able to carry out all usual activities, despite some symptoms. Score 2: Slight disability. Able to look after own affairs without assistance, but unable to carry out all previous activities. Score 3: Moderate disability. Requires some help, but able to walk unassisted. Score 4: Moderately severe disability. Unable to attend to own bodily needs without assistance, and unable to walk unassisted. Score 5: Severe disability. Requires constant nursing care and attention, bedridden, incontinent. Score 6: Dead)

Time frame
90 (±14) days post-treatment
2

Asymptomatic Intracranial Hemorrhage

Incidence of any asymptomatic intracranial hemorrhage post-procedure

Time frame
Day 1 (within 24 hours (18-36 hours) of the procedure)
3

Neurological Deterioration

Safety (defined as a ≥4-point increase in the National Institutes of Health Stroke Scale (NIHSS) score)

Time frame
Day 1 (within 24 hours (18-36 hours) of the procedure)

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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