Perfusion Imaging Evaluation for Ischemic Stroke on 6-24 Hours Undergoing Endovascular Thrombectomy

NCT ID: NCT03502408

Last Updated: 2022-11-23

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 55 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-08-01
• Study Completion Date: 2026-08-01

Brief Summary

This study aims to evaluate the hypothesis that thrombectomy devices plus medical management leads to superior clinical outcomes in acute ischemic stroke patients at 90 days as compared to medical management alone in appropriately selected subjects with the Target Mismatch Profile and an MCA (M1 and M2 segment) or ICA occlusion or BA who have endovascular thrombectomy initiated between 6-24 hours after last seen well.

Detailed Description

Study design is a prospective, single-center study of acute ischemic stroke patients with large artery occlusion in 6-24 hours of stroke onset. According to patients or their family members' willing, patients who meet the inclusion criteria will be assigned to endovascular thrombectomy group with approved devices (only the devices listed in this protocol are approved for us) plus standard medical therapy or control group (standard medical therapy alone) after undergoing either CT Perfusion or MR Perfusion studies. Patients who have evidence of an ICA or MCA M1 or M2 or BA occlusion and a Target Mismatch Profile will be enrolled.

The intent of this study is to support thrombectomy beyond the currently labeled 8 hour indicated time limit in wake up, unclear onset, and late presenting ischemic stroke subjects, who currently have no other option besides medical management of their symptoms, with careful selection.

The study will enroll up to 55 patients. The primary endpoint, the modified Rankin Score, will be assessed at 3 months.

Conditions

Stroke, Acute Cerebral Infarction

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Endovascular Thrombectomy

Procedure: Endovascular Thrombectomy Device: Trepo trevor Retriever Device: Solitaire™ FR Revascularization Device

Group Type: EXPERIMENTAL

Endovascular Thrombectomy

Intervention Type: PROCEDURE

Procedure: Endovascular Thrombectomy Device: Trepo trevor Retriever Device: Solitaire™ FR Revascularization Device

Endovascular Thrombectomy

Intervention Type: PROCEDURE

Procedure:Endovascular Thrombectomy Device: Solitaire™ FR Revascularization Device

Interventions

Endovascular Thrombectomy

Procedure: Endovascular Thrombectomy Device: Trepo trevor Retriever Device: Solitaire™ FR Revascularization Device

Intervention Type: PROCEDURE

Endovascular Thrombectomy

Procedure:Endovascular Thrombectomy Device: Solitaire™ FR Revascularization Device

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

1. Clinical signs and symptoms consistent with the diagnosis of an acute ischemic stroke

2. Age ≥18 years

3. NIHSS ≥ 6

4. Endovascular thrombectomy can be initiated (femoral puncture) between 6 and 24 hours after time last know well

5. No significant pre-stroke disability (pre-stroke mRS must be ≤ 3 )

6. Patient/Legally Authorized Representative has signed the Informed Consent form

1. ICA or MCA-M1 or MCA-M2 or BA occlusion (carotid occlusions can be cervical or intracranial with or without tandem MCA lesions) as evidenced by MRA or 4D-CTA

2. Target Mismatch Profile on CT perfusion or MR perfusion: ischemic core volume is ≤ 70 ml, mismatch ratio is >/= 1.2 )

Exclusion Criteria

1. Other serious, advanced, or terminal illness (investigator judgment) or life expectancy is less than 90 days

2. Subject with a co-morbid disease or condition that would confound the neurological and functional evaluations or compromise survival or ability to complete follow-up assessments

3. Unable to undergo a contrast brain perfusion scan with either MRI or CT

4. Pregnant

5. Known serious sensitivity to radiographic contrast agents

6. Treated with rtPA >6 hours after time last known well

7. Known hereditary or acquired hemorrhagic diathesis, coagulation factor deficiency; recent oral anticoagulant therapy with INR > 3 (recent use of one of the new oral anticoagulants is not an exclusion if estimated GFR > 30 ml/min).

8. Seizures at stroke onset if it precludes obtaining an accurate baseline NIHSS

9. Current participation in another investigational drug or device treatment study

10. Known hereditary or acquired hemorrhagic diathesis, coagulation factor deficiency

11. Any other condition that, in the opinion of the investigator, precludes an endovascular procedure or poses a significant hazard to the subject if an endovascular procedure was performed.

1. ASPECTS score <6 on non-contrast CT (if patient is enrolled based on CT perfusion criteria)

2. Evidence of intracranial tumor (except small meningioma), acute intracranial hemorrhage, neoplasm, subarachnoid hemorrhage, or arteriovenous malformation

3. Significant mass effect with midline shift

4. Evidence of internal carotid artery dissection

5. Intracranial stent implanted in the same vascular territory, known history of arterial tortuosity, and/or other arterial disease that precludes the safe deployment/removal of the thrombectomy device

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Second Affiliated Hospital, School of Medicine, Zhejiang University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

MIN LOU, Ph.D.

Role: STUDY_DIRECTOR

Second Affiliated Hospital, School of Medicine, Zhejiang University

Locations

Second Affiliated Hospital, School of Medicine, Zhejiang University

Hangzhou, Zhejiang, China

Site Status: RECRUITING

Countries

China

Central Contacts

MIN LOU, Ph.D.

Role: CONTACT

loumingxc@vip.sina.com

8657187784811

Facility Contacts

MIN LOU, Ph.D.

Role: primary

loumingxc@vip.sina.com

8657187784811

Other Identifiers

yan2017-150

Identifier Type: -

Identifier Source: org_study_id