REVASCAT: Endovascular Revascularization With Solitaire Device Versus Best Medical Therapy in Anterior Circulation Stroke Within 8 Hours

Sponsor

Fundacio Ictus Malaltia Vascular (Other)

Overall Status

Terminated

CT.gov ID

NCT01692379

Collaborator

Medtronic - MITG (Industry)

206

Enrollment

Locations

Arms

Duration (Months)

51.5

Patients Per Site

1.4

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

To evaluate the hypothesis that mechanical embolectomy with the Solitaire FR device is superior to medical management alone in achieving favorable outcome in the distribution of the modified Rankin Scale scores at 90 days in subjects presenting with acute large vessel ischemic stroke < 8 hours from symptom onset.

Condition or Disease	Intervention/Treatment	Phase
Acute Stroke	Device: Solitaire FR device Other: Medical treatment	Phase 3

Detailed Description

Prospective, multi-center, randomized, controlled, open, blinded-endpoint trial with a sequential design. The randomization employs a 1:1 ratio of mechanical embolectomy with the CE MARK approved stentriever Solitaire FR® versus medical management alone. Randomization will be done under a minimization process using age, baseline NIHSS, therapeutic window and vessel occlusion site. For the primary endpoint, subjects will be followed for 90 days post-randomization.

Interim analysis will be performed as preplanned and interpreted by the Data Safety Monitoring Board (DSMB) after the first 174, 346 and 518 patients representing 25%, 50% and 75% of the planned sample size have completed their 90-day follow-up. The DSMB will advise the executive committee (EC) on recommendations to stop the trial early either for reasons of safety, efficacy, futility or to adjust the sample size. The latter may be necessary as given the paucity of data regarding natural history of the non-treated patients assumptions regarding rates of favorable outcomes in this group of patients may be incorrect. Of note, sample size adjustment based on different than expected outcomes rates is permitted, but it is not permitted to adjust the sample size based on change in the pre-specified treatment effect which is set at 10%.

Subject population: Subjects presenting with acute ischemic stroke within 8 hours from symptom onset and whose strokes are attributable to an occlusion of the internal carotid or proximal MCA (M1) arteries. Subjects are either ineligible for IV alteplase or have received IV alteplase therapy without recanalization.

Study Design

Study Type:

Interventional

Actual Enrollment :

206 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

Single (Outcomes Assessor)

Primary Purpose:

Treatment

Official Title:

RandomizEd Trial of reVascularizAtion With Solitaire FR® Device Versus Best mediCal Therapy in the Treatment of Acute Stroke Due to anTerior Circulation Large Vessel Occlusion Presenting Within 8 Hours of Symptom Onset

Study Start Date :

Nov 1, 2012

Actual Primary Completion Date :

Mar 1, 2015

Actual Study Completion Date :

Dec 1, 2015

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Endovascular treatment Mechanical embolectomy with Solitaire FR device	Device: Solitaire FR device Mechanical embolectomy in anterior large vessel occlusion
Active Comparator: Medical treatment Medical treatment (standard of care in acute ischemic stroke)including intravenous thrombolysis	Other: Medical treatment Standard of care in acute ischemic stroke including intravenous rTPA

Arm

Intervention/Treatment

Experimental: Endovascular treatment

Mechanical embolectomy with Solitaire FR device

Device: Solitaire FR device

Mechanical embolectomy in anterior large vessel occlusion

Active Comparator: Medical treatment

Medical treatment (standard of care in acute ischemic stroke)including intravenous thrombolysis

Other: Medical treatment

Standard of care in acute ischemic stroke including intravenous rTPA

Outcome Measures

Primary Outcome Measures

Between-group comparison of the distribution of the modified Rankin Scale scores (shift analysis) [90 days after enrollment]
evaluated by two separate assessors who are blinded to treatment

Secondary Outcome Measures

Mortality at 90 days [90 days after enrollment]
Symptomatic Intracerebral Hemorrhage [24h (-2/+12 hours) after enrollment]
Deterioration in NIHSS score of ≥4 points within 24 hours from treatment and evidence of intraparenchymal hemorrhage type 2 in the 22 to 36 hours follow-up imaging scans evaluated by independent CT/MR Core Lab and Clinical Events Committee
Infarct Volume [24h (-2/+12h) post treatment]
Infarct volume evaluated in a second neuroimaging after treatment evaluated by independent CT/MR Core Lab
Vessel recanalization [24h post treatment]
Vessel recanalization evaluated by CT angiography or MRA at 24 hours in both treatment groups evaluated by independent CT/MR Core Lab
Intraprocedural related complications in endovascular arm [During endovascular treatment]
Procedural related complications in the endovascular treatment arm: arterial perforation, arterial dissection, and embolization in a previously uninvolved vascular territory evaluated by the Angiography Core Lab and the Clinical Events Committee

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 85 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

1. Acute ischemic stroke where patient is ineligible for IV thrombolytic treatment or the treatment is contraindicated (e.g., subject presents beyond recommended time from symptom onset), or where patient has received IV thrombolytic therapy without recanalization after a minimum of 30 min from start of iv tPA infusion
1. No significant pre-stroke functional disability (mRS ≤ 1)
1. Baseline NIHSS score obtained prior to randomization must be equal or higher than 6 points
1. Age ≥18 and ≤ 85.
1. Occlusion (TICI 0-1) of the intracranial ICA (distal ICA or T occlusions), MCA-M1 segment or tandem proximal ICA/MCA-M1 suitable for endovascular treatment, as evidenced by CTA, MRA or angiogram, with or without concomitant cervical carotid occlusion or stenosis
1. Patient treatable within eight 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 groin puncture.
1. Informed consent obtained from patient or acceptable patient surrogate

Exclusion Criteria:

Clinical criteria
1. Known hemorrhagic diathesis, coagulation factor deficiency, or oral anticoagulant therapy with INR > 3.0
1. Baseline platelet count < 30.000/µL
1. Baseline blood glucose of < 50mg/dL or >400mg/dl
1. Severe, sustained hypertension (SBP > 185 mm Hg or DBP > 110 mm Hg)
1. Patients in coma (NIHSS item of consciousness >1) (Intubated patients for transfer could be randomized only in case an NIHSS is obtained by a neurologist prior transportation).
1. Seizures at stroke onset which would preclude obtaining a baseline NIHSS
1. Serious, advanced, or terminal illness with anticipated life expectancy of less than one year.
1. History of life threatening allergy (more than rash) to contrast medium
1. Subjects who has received iv t-PA treatment beyond 4,5 hours from the beginning of the symptoms
1. Renal insufficiency with creatinine ≥ 3 mg/dl
1. Woman of childbearing potential who is known to be pregnant or lactating or who has a positive pregnancy test on admission.
1. Subject participating in a study involving an investigational drug or device that would impact this study.
1. Cerebral vasculitis
1. Patients with a pre-existing neurological or psychiatric disease that would confound the neurological or functional evaluations, mRS score at baseline must be ≤

This excludes patients who are severely demented, require constant assistance in a nursing home type setting or who live at home but are not fully independent in activities of daily living (toileting, dressing, eating, cooking and preparing meals, etc.)

1. Unlikely to be available for 90-day follow-up (e.g. no fixed home address, visitor from overseas).

Neuroimaging criteria:

1. Hypodensity on CT or restricted diffusion amounting to an ASPECTS score of <7 on NCCT or <6 on DWI MRI. Patients 81 to 85 years old with ASPECTS score on non-contrast CT or DWI MRI <9 must be excluded. ASPECTS must be evaluated by CBV maps of CT Perfusion, CTA source imaging (CTA-SI) or DWI-MR in patients whose vascular occlusion study (CTA/MRA) confirming qualifying occlusion, is performed beyond 4.5 hours of last seen well.
1. CT or MR evidence of hemorrhage (the presence of microbleeds is allowed).
1. Significant mass effect with midline shift.
1. Evidence of ipsilateral carotid occlusion, high grade stenosis or arterial dissection in the extracranial or petrous segment of the internal carotid artery that cannot be treated or will prevent access to the intracranial clot or excessive tortuosity of cervical vessels precluding device delivery/deployment
1. Subjects with occlusions in multiple vascular territories (e.g., bilateral anterior circulation, or anterior/posterior circulation)
1. Evidence of intracranial tumor (except small meningioma).

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Hospital Germans Trias i Pujol	Badalona	Barcelona	Spain	08916
2	Hospital Universitari Bellvitge	Hospitalet de Llobregat	Barcelona	Spain	08907
3	Hospital Universitario Vall D'Hebron	Barcelona		Spain	08035
4	Hospital Clinic	Barcelona		Spain	08036

Sponsors and Collaborators

Fundacio Ictus Malaltia Vascular
Medtronic - MITG

Investigators

Study Chair: Antoni Dávalos, MD, Hospital Universitario Germans Trias i Pujol, Barcelona, Spain
Study Chair: Tudor Jovin, MD, UPMC Stroke Institute, Pittsburgh, PA, USA
Study Director: Angel Chamorro, MD, Hospital Clinic Barcelona, Barcelona, Spain
Study Director: Joaquin Serena, MD, Hospital Josep Trueta, Girona, Spain
Study Director: Alex Rovira, MD, Hospital Vall D'Hebron, Barcelona, Spain
Study Director: Maria A De Miquel, MD, Hospital de Bellvitge, Barcelona, Spain
Study Director: Luis Sanromán, MD, Hospital Clinic, Barcelona, Spain
Study Director: Erik Cobo, MD, UPC, Barcelona, Spain
Study Director: Carlos Molina, MD, Hospital Vall D'Hebron, Barcelona, Spain