Aggressive Medical Treatment Evaluation for Asymptomatic Carotid Artery Stenosis (AMTEC)

This study is currently recruiting participants.
Verified June 2011 by Russian Cardiology Research and Production Center
Sponsor:
Collaborator:
Krka, d.d., Novo mesto, Slovenia
Information provided by:
Russian Cardiology Research and Production Center
ClinicalTrials.gov Identifier:
NCT00805311
First received: December 8, 2008
Last updated: June 14, 2011
Last verified: June 2011

December 8, 2008
June 14, 2011
April 2009
September 2012   (final data collection date for primary outcome measure)
Major adverse cardiovascular events (MACE: composite of stroke, myocardial infarction and cardiovascular death) and any death [ Time Frame: 5 years ] [ Designated as safety issue: Yes ]
Major adverse cardiovascular events (MACE: composite of stroke, myocardial infarction and cardiovascular death) and any death [ Time Frame: 24 months ] [ Designated as safety issue: Yes ]
Complete list of historical versions of study NCT00805311 on ClinicalTrials.gov Archive Site
Restenosis after CEA [ Time Frame: 5 years ] [ Designated as safety issue: No ]
Restenosis after CEA [ Time Frame: 24 months ] [ Designated as safety issue: No ]
Not Provided
Not Provided
 
Aggressive Medical Treatment Evaluation for Asymptomatic Carotid Artery Stenosis
Carotid Endarterectomy Versus Optimal Medical Treatment of Asymptomatic High Grade Carotid Artery Stenosis

The aim of this study is to determine whether optimal medical treatment can postpone carotid endarterectomy.

It is well known that risk of fatal and non-fatal stroke is increased in patients with significant carotid atherosclerosis. For asymptomatic patients, AHA guidelines recommend carotid endarterectomy (CEA) for stenosis 60% to 99%, if the risk of perioperative stroke or death is less than 3%.

Although clinical trial data support CEA in asymptomatic patients with carotid stenosis 60% to 79%, the AHA guidelines indicate that some physicians delay revascularization until there is greater than 80% stenosis in asymptomatic patients.

Our study is designed to determine whether optimal medical therapy alone reduces the risk of death and nonfatal stroke in patients with carotid artery stenosis as compared with CEA coupled with optimal medical therapy.

Interventional
Phase 4
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Prevention
  • Carotid Artery Stenosis
  • Atherosclerosis
  • Stroke
  • Procedure: Carotid Endarterectomy
    CEA involves a neck incision and physical removal of the plaque from the inside of the artery
  • Drug: atorvastatin, aspirin, losartan, amlodipine
    aspirin 100 mg/day, atorvastatin 10 mg/day, losartan 50 mg/day, amlodipine 5 mg/day
  • Experimental: 1
    Patients receive medical treatment including medical therapy with statins (at least 10 mg atorvastatin irrespective of the baseline cholesterol level), aspirin (100 mg daily) and antihypertensive therapy (at least 50 mg losartan and 5 mg amlodipine 75 mg daily irrespective of the baseline arterial pressure level). Further conservative medical treatment includes modification of cardiovascular risk factors according to current recommendations. Additionally patients will undergo CEA.
    Interventions:
    • Procedure: Carotid Endarterectomy
    • Drug: atorvastatin, aspirin, losartan, amlodipine
  • Active Comparator: 2
    Patients receive medical treatment including medical therapy with statins (at least 10 mg atorvastatin irrespective of the baseline cholesterol level), aspirin (100 mg daily) and antihypertensive therapy (at least 50 mg losartan and 5 mg amlodipine 75 mg daily irrespective of the baseline arterial pressure level). Further conservative medical treatment includes modification of cardiovascular risk factors according to current recommendations.
    Intervention: Drug: atorvastatin, aspirin, losartan, amlodipine
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
150
October 2017
September 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Unilateral or bilateral carotid artery stenosis that was considered to be severe (carotid artery diameter reduction 70%-79% on ultrasound)
  • This stenosis had not caused any stroke, transient cerebral ischaemia, or other relevant neurological symptoms in the past 6 months
  • Both doctor and patient were substantially uncertain whether to choose immediate CEA, or deferral of any CEA until a more definite need for it was thought to have arisen
  • The patient had no known circumstance or condition likely to preclude long-term follow-up
  • Neurologist's explicit consent to potentially perform CEA

Exclusion Criteria:

  • Previous ipsilateral CEA
  • Expectation of poor surgical risk (e.g., because of recent acute myocardial infarction)
  • Some probable cardiac source of emboli (because the main stroke risk might then be from cardiac, not carotid, emboli)
  • Inability to provide informed consent
  • Underlying disease other than atherosclerosis (inflammatory or autoimmune disease)
  • Life expectancy < 6 months
  • Advanced dementia
  • Advanced renal failure (serum creatinine > 2.5 mg/dL)
  • Unstable severe cardiovascular comorbidities (e.g., unstable angina, heart failure)
  • Restenosis after prior CAS or CEA
  • Allergy or contraindications to study medications (statins, ASA, losartan, amlodipine)
Both
40 Years to 80 Years
No
Contact: Igor Kolos, PhD 414-6201 ext +7(495) docsn173@yandex.ru
Contact: Sergey Boytsov, MD 149-0141 ext +7(499) prof-boytsov@mail.ru
Russian Federation
 
NCT00805311
NCT00805311
Yes
Anna Zakharova, KRKA d.d. Novo mesto, Slovenia
Russian Cardiology Research and Production Center
Krka, d.d., Novo mesto, Slovenia
Study Chair: Evgeniy Chazov, MD Russian Cardiology Research and Production Center
Russian Cardiology Research and Production Center
June 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP