Ultrasound Enhanced Thrombolytic Therapy of Middle Cerebral Artery Occlusion

Phase 3

• Conditions: Intracranial Embolism; Thrombosis

• Registration Number: NCT00336596
• Lead Sponsor: University of Zurich

Brief Summary

The purpose of the present, randomized, controlled multicenter phase III trial is to investigate the safety and efficacy of continuous 1-hour insonation of occluded middle cerebral artery with 2 MHz TCCS in stroke patients treated with intravenous tissue plasminogen activator (t-PA) within 3 hours after symptom onset.

Detailed Description

Thrombolysis with intravenous(iv) tissue plasminogen activator (t-PA) is the only effective and approved therapy for acute ischemic stroke. The most frequent cause of ischemic stroke is thrombosis of the middle cerebral artery (MCA). Preliminary in vitro, animal and human studies suggest that ultrasound accelerates thrombolysis induced by t-PA, and recanalization of acute MCA occlusion due to thrombolysis is an independent predictor of good clinical outcome. Thus, insonation of an occluded MCA through the temporal bone in stroke patients who are treated with iv t-PA might enhance recanalization and improve clinical outcome. The present prospective, randomized, controlled multicenter pilot study will investigate the safety and efficacy of continuous 1-hour insonation of the occluded MCA with 2 MHz transcranial color duplex sonography in patients with ischemic stroke treated with iv t-PA within 3 hours after symptom onset. It is planned to randomize 400 patients in 6 Swiss centers during an enrolment period of 33 months with an individual follow up of 3 months. The study endpoints include safety and efficacy assessments. The primary safety endpoint is to determine the rate of symptomatic intracranial hemorrhage (ICH) in both treatment groups. The primary efficacy endpoint is to determine whether a good functional outcome (modified Rankin scale, mRs, score of 0-2) differs between both treatment groups. Secondary endpoints include (1) asymptomatic ICH occuring during or within the first 24-48 hours after t-PA infusion, (2) early clinical recovery by 10 or more National Institute of Health Stroke Scale (NIHSS) points or dramatic recovery (total NIHSS score of 3 or less) at 24-48 hours after t-PA infusion, (3) mean mRS score at 90 days after t-PA infusion, (4) death occuring during the study period, and (5) recanalization at 24-48 hours after t-PA infusion.

Study Timeline

• Study Start: 2006-06
• Study First Submitted: 2006-06-13
• Study First Submitted QC: 2006-06-13
• Study First Posted: 2006-06-14
• Status Verified: 2007-04
• Last Update Submitted: 2007-04-25
• Last Update Posted: 2007-04-27
• Study Completion: 2009-06

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 400

Inclusion Criteria

• acute ischemic stroke in the MCA territory according to clinical and cranial computed tomography (CT) or cranial MR imaging (MRI) findings
• patient undergoing iv thrombolysis with t-PA within 3 hours after stroke onset
• Occlusion of sphenoidal (M1) or insular (M2) segment of the MCA at CT (CTA), MR (MRA) or catheter (CA) angiography
• appropriate temporal bony window without echocontrast agents for insonation with TCCS
• full functional independence prior to present stroke (mRS 0-1), use of a cane for walking due to comorbid condition is acceptable
• written informed consent, signed and dated by the subject (or subject's authorized representative, if allowed by local laws) and by the person obtaining the consent, indicating agreement to comply with all protocol-specific procedures

Exclusion Criteria

• unconsciousness (more than 2 points on item 1a on NIHSS)
• history of intracranial hemorrhage, arteriovenous malformation or aneurysm
• severe cranio-cerebral trauma within the last 3 months
• symptoms of subarachnoidal hemorrhage
• time of symptom onset unclear
• large surgical intervention or trauma within the last 10 days
• expected survival below 90 days after iv t-PA treatment
• severe hepatic disease, esophageal varices, acute pancreatitis
• septic embolism, endocarditis, pericarditis after myocardial infarction
• pregnancy or childbirth within the last 30 days or nursing mothers
• history of hemorrhagic diathesis or coagulopathy
• untreatable increase of arterial blood pressure (>185mmHg systolic, >110mmHg diastolic)
• intracranial hemorrhage, arteriovenous malformations or aneurysm at brain imaging
• thrombocytes <100'000 per microliter
• international normalized ratio (INR)>1.7 or partial thromboplastin time (PTT) prolongated
• serum glucose <2.7mmol/l or >22.2mmol/l
• severe renal insufficiency or other contraindications against CT-contrast agents

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Symptomatic intracranial hemorrhage (safety)
Functional outcome (efficacy)

Secondary Outcome Measures

Name	Time	Method
Asymptomatic intracranial hemorrhage 24-48 hours after t-PA infusion
Early clinical recovery by 10 or more NIHSS points or dramatic recovery (total NIHSS 3 or less)at 24-48 hours after t-PA infusion
Mean mRS score at 90 days after t-PA infusion
Death occurring during study period
Recanalization at 24-48 hours after t-PA infusion

Trial Locations

Locations (6)

University Hospital of Lausanne, Department of Neurology; 🇨🇭 Lausanne, Switzerland

Kantonsspital Aarau, Department of Neurology; 🇨🇭 Aarau, Switzerland

University Hospital of Geneva, Department of Neurology; 🇨🇭 Geneva, Switzerland

University Hospital of Basel, Department of Neurology; 🇨🇭 Basel, Switzerland

University Hospital of Zurich, Department of Neurology; 🇨🇭 Zurich, Switzerland

University hospital of Bern, Department of Neurology; 🇨🇭 Bern, Switzerland