Concentric Retriever Device (CRD) in Acute Ischemic Stroke

NCT00203710 | Completed

• 1 other identifier: UCLA-TR-001
• Study Type: interventional
• Target: 50
• Locations: 1 country
• Sites: 1

Brief Summary

The primary purpose is to study the safety and effectiveness of the Concentric Retriever Device(CRD)in ischemic stroke patients who undergo clot retrieval with the CRD within 8 hours of stroke symptom onset. The CRD has been approved by the U.S. Food and Drug Administration to retrieve foreign bodies (such as pieces of metal) from blood vessels in the body. The CRD is a small metal wire with a loop at the end (like a corkscrew) that removes clots from arteries and thereby restores blood flow to the brain. Prior versions of the CRD may have been too soft to pull out clots, just as a corkscrew that is too soft would not pull out corks. The current version of the CRD is not as soft and may be more effective in retrieving clots. Hypothesis: By restoring blood flow to the brain, stroke symptoms may get better or the stroke may be prevented from getting worse.

Conditions

Acute Ischemic Stroke

Keywords

Concentric Retriever Device; embolectomy; acute ischemic stroke; treatment

Outcome Measures

Primary Outcomes (2)

• Achievement of recanalization (TIMI/TICI grade II or III flow) immediately post procedure.

• In addition, major complications defined as vessel perforation, intramural arterial dissection, symptomatic intra-cranial hemorrhage, and significant embolization in a previously uninvolved arterial territory will be tabulated.

Secondary Outcomes (3)

• Assessment of patient's neurological condition and functional state using the NIHSS, Barthel Index, and

• Modified Rankin at 30 and 90 days post-procedure.

• A composite of major adverse events at 30 and 90 days post-procedure. Major adverse events are defined as death and new stroke.

Interventions

Concentric Retriever Device DEVICE

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• (a) -Patients who present within 8 hours of stroke onset and are not candidates for treatment with t-PA who have clinical signs consistent with the diagnosis of ischemic stroke such as impairment of language, motor function, sensation, cognition, and/or gaze, or vision.
• (b). Patients who have had an acute ischemic stroke treated with intravenous thrombolytic therapy where vascular imaging (TCD, CTA, MRA, angiography) shows a persistent occlusion after the end of the infusion treatment.
• \. Patients \> 18 years of age. 3. NIHSSS \> 7 4. Angiogram shows a thrombotic occlusion originating in the internal carotid, middle cerebral (M1 or M2 segment), basilar, posterior cerebral, or vertebral arteries.
• \. Patient/patient guardian is willing to comply with the protocol requirements and return to the treatment center for all required clinical evaluations.

You may not qualify if:

• Patient is pregnant (if within child bearing age).
• Patient has baseline glucose of \< 50mg/dL (\<50 mg/mM).
• Patient has excessive arterial tortuosity that precludes the device from reaching the target area.
• Patient has known hemorrhagic diathesis, coagulation factor deficiency, or oral anticoagulant therapy with INR \> 2.0.
• Patient received Heparin within 48 hours with a PTT greater than 2 times the lab normal.
• Patient has baseline platelets \< 30,000.
• Patient has history of severe allergy to intra-arterial contrast medium.
• Patient has severe, sustained hypertension (systolic blood pressure \> 185 mm Hg or diastolic blood pressure \> 110 mm Hg).
• NOTE: If the blood pressure can be successfully reduced and maintained at the acceptable level using medication (i.e. Nipride), the patient can be enrolled.
• CT Scan or MRI reveals significant mass effect with midline shift.
• Patient's angiogram shows an arterial stenosis (\>50%) proximal to the embolus.
• Patient's anticipated life expectancy is less than 3 months.

Sponsors & Collaborators

• Sidney Starkman: lead

Study Sites (1)

University of California, Los Angeles

Los Angeles, California, 90024, United States

Location

MeSH Terms

Conditions

Ischemic Stroke

Condition Hierarchy (Ancestors)

Stroke; Cerebrovascular Disorders; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Vascular Diseases; Cardiovascular Diseases

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR INVESTIGATOR
• PI Title: Clinical Professor, Emergency Medicine and Neurology

Study Record Dates

• First Submitted: September 13, 2005
• First Posted: September 20, 2005
• Study Start: October 1, 2003
• Primary Completion: September 1, 2004
• Study Completion: September 1, 2004
• Last Updated: December 14, 2015

Record last verified: 2015-12

Locations

US (1)