Cerebral Stroke, Cerebrovascular Stroke, Stroke, Acute
Conditions
Keywords
Acute Ischemic Stroke, Thrombectomy, Aspiration Thrombectomy, Observational study
Brief summary
Sesame is a European, multi-center, single arm, prospective, observational registry. Sesame aims to demonstrate that use of SOFIA™/SOFIA™ PLUS catheter for direct aspiration as a first line treatment technique is fast, safe and effective in patients suffering an Acute Ischemic Stroke when assessed at 24 hours, discharge and 90 days after treatment. 250 patients will be enrolled. All patients will be followed for 90 days or until death.
Detailed description
Several publications describing the use of aspiration as a first line treatment technique in AIS patients have shown superior technical results with similar clinical outcomes to those seen when using a traditional stent retriever. They have also shown decreased procedure time and cost. The aim of this study is to show similar results in terms of speed, Effectiveness and safety when SOFIA™/ SOFIA™ PLUS is the catheter used for first line aspiration thrombectomy. The SOFIA™ (Soft Torqueable Catheter Optimized For Intracranial Access) and SOFIA™ PLUS Catheter are single lumen, flexible catheters, designed with coil and braid reinforcement. The SOFIA™ / SOFIA™ PLUS catheters have a soft distal tip for easy navigation in tortuous vessels. The tip is steam shapable and the proximal shaft torquable to help steer around challenging bifurcations. The coil and braid construction provides enhanced kink resistance and 1:1 push / pull control. Once navigated to the site of the occlusion, the SOFIA™ / SOFIA™ PLUS catheters can be used in conjunction with an aspiration source, such as a pump or syringe, to facilitate aspiration thrombectomy of the occluded vessel. The SOFIA™ / SOFIA™ PLUS catheters have large lumens, developed to maximize aspiration power and capture of thrombus. SESAME is a multi-center, single arm, prospective, observational registry of the SOFIA™/ SOFIA™ PLUS Catheter in Europe. Consecutive patients presenting within 6 hours of symptom onset with an anterior circulation large vessel occlusion (LVO) acute ischemic stroke (within the internal carotid artery and internal carotid terminus, middle cerebral -M1/M2 segments) will be treated using aspiration thrombectomy as first intention and site routine practice. Devices received CE-mark and will be used according to the 'Instructions For Use'. The follow-up visits will occur at 24 +/- 12 hours, at patient discharge, and 90+/-14 days post-procedure. Furthermore the study design is adaptive, prospectively stating interim analyses with specified stopping rules, which allow for the possibility of the study to terminate early based on either a determination of study success or of the futility to continue further enrollment.
Interventions
DEVICESofia
The SOFIA™/ SOFIA™ PLUS Catheter will be used in removal/aspiration of emboli and thrombi following the CE marked Instructions For Use. Enrollment into the study does not change the routine care at the site provided to the patient requiring mechanical thrombectomy treatment.
Sponsors
Microvention-Terumo, Inc.
Eppdata Hamburg
Dr. Markus Alfred Möhlenbruch
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Participant is ≥ 18 2. Demonstrated occlusion of the distal intracranial carotid artery, middle cerebral artery (M1 or M2) or anterior cerebral artery (A1 or A2) proven by CT and/or MRI 3. NIHSS ≥ 2 and ≤ 30 at screening 4. Start of the thrombectomy procedure within 6 hours of the onset of stroke symptoms 5. Pre event mRS ≤1 6. Patient or patient's legally authorized representative has received information about data collection and has signed and dated an Informed Consent Form
Exclusion criteria
1. Patient is more than 6 hours from symptom onset 2. Rapidly improving neurologic examination 3. Evidence of cerebral ischemia in the posterior circulation 4. Severe unilateral or bilateral carotid artery stenosis requiring stent treatment 5. Presence of an existing or pre-existing large territory infarction 6. Absent femoral pulses 7. Excessive vascular tortuosity that will likely result in unstable access 8. Pregnancy; if a woman is of child-bearing potential a urine or serum beta HCG test is positive 9. Known contrast product allergy 10. Patient has a severe or fatal comorbidity that will likely prevent improvement or follow up or that will render the procedure unlikely to benefit the patient 11. Evidence of intracranial hemorrhage (SAH, ICH, etc.) Imaging
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Clinical outcome | 90 days | Dichotomization of patients into good functional outcome defined as a modified Rankin Score (mRS) ≤ 2 and bad functional outcome defined as mRS \>2 |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Safety - procedural | 90 days | Devices and procedure related adverse events within 90 days of follow up |
| ENT | Intra-procedure | Infarct in a New Territory After Treatment Administration as seen on final control angiogram at the end of the procedure |
| sICH | 24 hours | Occurrence of symptomatic intracranial hemorrhage (sICH) within 24 hours |
| Vessel damage | Intra-procedure | Occurrence of intracranial vessel damage at the end of the procedure as seen on final control angiogram at the end of the procedure |
| Recanalization - Aspiration | Intra-procedure | Proportion of patients having complete recanalization (TICI≥ 2b) just after first line aspiration treatment as seen on control angiogram |
| Safety - neurological | Prior to discharge / approximated 3-7 days | Occurrence of major neurological events (stroke, intracranial hemorrhage, intracerebral hemorrhage, etc.) |
| Recanalization - Other | Intra-procedure | Proportion of patients having complete recanalization (TICI ≥ 2b) af-ter thrombectomy using an additional devices as seen on control angiogram |
| Time to recanalization- Aspiration | Intra-procedure | Time from groin puncture to complete recanalization (TICI ≥ 2b) in patients after first line aspiration treatment as seen on control angiogram |
| Time to recanalization- Other | Intra-procedure | Time from groin puncture to complete recanalization (TICI ≥ 2b) in patients after thrombectomy using an additional device as seen on control angiogram |
| Time to angio | Intra-procedure | Time from CT-scan/MRI at the institution to groin access |
| Degree of disability - discharge | Discharge/ approximately 3-7 days | modified Rankin Score at discharge, total score |
| Neurological outcome 24 | 24 hours | National Institutes of Health Stroke Scale (NIHSS) score at 24 hours, total and subscale scores |
| Neurological outcome discharge | Discharge / approximately 3-7 days | National Institutes of Health Stroke Scale (NIHSS) score at discharge, total and subscale scores |
| Neurological outcome 90 days | 90 days / +/- 14 days | National Institutes of Health Stroke Scale (NIHSS) score at 90 days, total and subscale scores |
| Degree of disability - 90d | 90 days / +/- 14 days | modified Rankin Score at 90 day follow-up, total score |
| Quality of Life at 90 days | 90 days / +/- 14 days | Quality of Life at 90 days assessed via PROMIS Scale v1.2 - Global Health, total score |
| Imaging | 24 hours | Difference of Alberta stroke program early CT score (ASPECTs) scores in CT/MRI pretreatment vs. 24h, total scores |
| Imaging - perfusion | 24 hours | In the subgroup of patients with additional perfusion CT (as per local standard of care): volume of saved brain tissue determined by predictive modeling |
| Health Economics -device | Intra-procedure | Device costs (standardized cost of all devices as well as human resources and medication used during index procedure) |
| Health Economics - hospital | Discharge / approximately 3-7 days | Hospital length of stay |
| Symptom onset | Pre-procedure | Time from symptom onset to CT-scan/MRI |
Countries
Austria, France, Germany, Italy, Netherlands
Outcome results
None listed