Tracking Information
Start Date ICMJE | April 2009 |
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Estimated Primary Completion Date | April 2011 (final data collection date for primary outcome measure) |
Current Primary Outcome Measures ICMJE (submitted: December 8, 2008) | 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 ] |
Original Primary Outcome Measures ICMJE | Same as current |
Change History | Complete list of historical versions of study NCT00805311 on ClinicalTrials.gov Archive Site |
Current Secondary Outcome Measures ICMJE (submitted: December 8, 2008) | Restenosis after CEA [ Time Frame: 24 months ] [ Designated as safety issue: No ] |
Original Secondary Outcome Measures ICMJE | Same as current |
Descriptive Information
Brief Title ICMJE | Aggressive Medical Treatment Evaluation for Asymptomatic Carotid Artery Stenosis |
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Official Title ICMJE | Carotid Endarterectomy Versus Optimal Medical Treatment of Asymptomatic High Grade Carotid Artery Stenosis |
Brief Summary | The aim of this study is to determine whether optimal medical treatment can postpone carotid endarterectomy. |
Detailed Description | 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. |
Study Phase | Phase IV |
Study Type ICMJE | Interventional |
Study Design ICMJE | Prevention, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study |
Condition ICMJE |
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Intervention ICMJE |
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Study Arms / Comparison Groups |
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Recruitment Information
Estimated Enrollment ICMJE | 150 | ||||||||
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Estimated Completion Date | April 2011 | ||||||||
Estimated Primary Completion Date | April 2011 (final data collection date for primary outcome measure) | ||||||||
Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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Gender | Both | ||||||||
Ages | 40 Years to 80 Years | ||||||||
Accepts Healthy Volunteers | No | ||||||||
Contacts ICMJE |
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Location Countries ICMJE | Russian Federation |
Administrative Information
NCT ID ICMJE | NCT00805311 | ||||
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Responsible Party | Anna Zakharova, KRKA d.d. Novo mesto, Slovenia | ||||
Study ID Numbers ICMJE | NCT00805311 | ||||
Study Sponsor ICMJE | Russian Cardiology Research and Production Center | ||||
Collaborators ICMJE | Krka, d.d., Novo mesto, Slovenia | ||||
Investigators ICMJE |
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Information Provided By | Russian Cardiology Research and Production Center |