STAMCAR: A Prospective EC-IC Bypass Registry

Lahey Health

Status: Withdrawn

Conditions: Carotid Occlusion

Treatments: Procedure: EC-IC bypass

Study type: Observational

Funder types: Other

Identifiers

NCT02779803

LCID: 2015-034

Details and patient eligibility

About

A prospective registry evaluating the efficacy of EC-IC bypass in a subgroup of patients, specifically, patients with carotid occlusion and symptoms refractory to medical therapy and evidence for poor cerebrovascular reserve as evaluated by physiological testing (e.g. Diamox Challenge SPECT Scan). This subgroup includes:

1. Hospitalized unstable patient with crescendo or postural TIA's
2. Patients with multiple TIA's, limb-shaking TIA's, and/or cognitive decline despite medical therapy.

Full description

The registry is a multi-center international prospective registry. The patients will be prospectively followed for 24 months. Enrollment into the registry will take place over 3 years.

The primary objective is to collect prospective data on cerebral revascularization via superficial temporal artery (STA) to middle cerebral artery (MCA) for symptomatic carotid occlusion patients to determine if the procedure can be performed with less than 8% major peri-operative benchmark.

The secondary objective is to determine if cerebral revascularization via STA to MCA bypass will improve cerebral hemodynamics, cognitive function, and quality of life in a defined subgroup of symptomatic carotid occlusion patients over a 2 year period.

Clinical outcome in terms of resolved symptomatology, improved cerebrovascular hemodynamics, and cognitive status will be assessed. Short term and long term follow-up for a period of 24 months will include assessment of ipsilateral stroke or TIA rate, mortality, graft patency, assessment of MCA and bypass flow rates (if available), cognitive evaluation and quality of life evaluation.

Following enrollment baseline demographics and operative data will be collected. Follow-up will be performed at 1 month (m), 3m, 6m, 12m and 24m. Occurrence of new TIA or stroke will be determined. The patient's bypass patency, Qualitative Magnetic Resonance Angiogram (QMRA) flow data (site discretion) and NIHSS Score (NIHSS), Barthel Index (mBARTHEL), modified Rankin Scales (mRANKIN), EuroQOL, and the Montreal Cognitive Assessment (MoCA) with digital Clock Drawing (dCDT) will be recorded. An additional battery of neurocognitive tests will also be administered (Symbol Digit Modalities Test SDMT, Delis-Kaplan Executive Function System D-KEFS and TRAILS A/B).

Sex: All

Ages: 18 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Internal carotid artery or middle cerebral artery occlusion

• Transient ischemic attack (TIA) or ischemic stroke in the ipsilateral hemisphere within 30 days in patients who are either

  • hospitalized unstable patients with crescendo or postural TIA's, OR
  • Multiple TIA's, limb-shaking TIA's, and/or cognitive decline despite medical therapy*

• Evidence of ipsilateral impaired cerebrovascular reserve on physiological testing (e.g. Diamox challenge SPECT)

• Modified Rankin Score (mRS) >3

• Language comprehension intact

• Age 18-85 years * failure of medical therapy must include at least failure on a regimen of antiplatelets and statins.

Exclusion criteria

• Moya-moya syndrome

• Known heart disease likely to cause cerebral ischemia

  • Prosthetic Valves
  • Atrial Fibrillation
  • Infective endocarditis
  • Left atrial or ventricular thrombus
  • Sick sinus syndrome
  • Cardiac myxoma
  • Cardiomyopathy with ejection fraction < 25%

• Any condition likely to lead to death within 2 years

• Pregnancy

• Allergy or contraindication to aspirin

• Uncontrolled diabetes mellitus (FBS > 300 mg%/16.7 mmol/L)

• Uncontrolled hypertension (systolic BP>180, diastolic BP >110), other than induced for control of pressure dependent symptoms

• Uncontrolled hypotension (diastolic BP <65)

• Unstable angina