VITATOPS: A Study of VITAmins TO Prevent Stroke
The VITATOPS study is a multi-center, randomized, double blind, placebo-controlled secondary stroke prevention trial to determine whether the addition of vitamin supplements (B12 500 ug, B6 25 mg, Folate 2 mg) to best medical/surgical management (including modification of risk factors) will reduce the combined incidence of recurrent vascular events (stroke, myocardial infarction) and vascular death in patients with recent stroke or transient ischemic attack (TIA). All patients presenting to one of the participating neurologists or general physicians within seven months of stroke (ischemic or hemorrhagic) or TIA (eye or brain) are eligible for this trial. Eligible patients will be randomized in a double-blind fashion to receive multi-vitamins or placebo, 1 tablet daily. The primary outcome event is the composite event "stroke, myocardial infarction, or death from any vascular cause", whichever occurs first. Our target is to recruit a total of 8,000 patients over the next two years with a median follow-up of 2.5 years. Recruitment to the trial began in November 1998 and is planned to continue until December 2005. We aim to complete final follow-up by the end of 2006. However, the Steering Committee will be flexible in dictating the need for ongoing recruitment and continuing follow-up, depending on the overall rate of the primary outcome event in the entire cohort at each interim analysis.
Transient Ischemic Attack
Other: folic acid
Dietary Supplement: Vitamin B6
Dietary Supplement: Vitamin B12
|Study Design:||Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Prevention
|Official Title:||VITATOPS - A Study of VITAmins TO Prevent Stroke|
- Non-fatal stroke [ Time Frame: trial end ] [ Designated as safety issue: Yes ]
- Non-fatal myocardial infarction [ Time Frame: trial end ] [ Designated as safety issue: Yes ]
- Death due to vascular causes [ Time Frame: trial end ] [ Designated as safety issue: Yes ]
- TIA [ Time Frame: trial end ] [ Designated as safety issue: Yes ]
- Revascularization procedures [ Time Frame: trial end ] [ Designated as safety issue: Yes ]
- Dementia [ Time Frame: trial end ] [ Designated as safety issue: Yes ]
- Depression [ Time Frame: trial end ] [ Designated as safety issue: Yes ]
|Study Start Date:||November 1998|
|Study Completion Date:||June 2009|
|Primary Completion Date:||June 2009 (Final data collection date for primary outcome measure)|
Other: folic acid
Background: Epidemiological studies suggest that raised plasma concentrations of total homocysteine (tHcy) may be a common, causal and treatable risk factor for atherothromboembolic ischemic stroke, dementia and depression. Although tHcy can be lowered effectively with small doses of folic acid, vitamin B12 and vitamin B6, it is not known whether lowering tHcy, by means of multivitamin therapy, can prevent stroke and other major atherothromboembolic vascular events, dementia and depression.
Purpose: To determine whether vitamin supplements (folic acid 2 mg, B6 25 mg, B12 500 ug) reduce the risk of stroke, other serious vascular events, dementia and depression in patients with recent stroke or transient ischemic attacks of the brain or eye (TIA).
Methods: An international, multi-center, randomized, double-blind, placebo-controlled clinical trial.
Subjects: Patients with stroke or TIA in the previous 7 months.
Primary outcome measure: Non-fatal stroke, non-fatal myocardial infarction, or death due to vascular causes.
Secondary outcome measures: TIA, Revascularisation procedures, Dementia, Depression.
Sample size calculation: To reliably identify a 15% reduction in relative risk of the primary outcome event from 8% to 6.8% per year with an alpha of 0.05 and power of 80%, 8,000 patients need to be randomized and followed-up for an average of two years.
Current progress: As of November, 2004, more than 4,400 patients have been randomized in 73 centers in 19 countries in five continents: Australia, Austria, Belgium, Brazil, Hong Kong, Italy, Malaysia, Moldova, Netherlands, New Zealand, Pakistan, Philippines, Portugal, Republic of Georgia, Serbia & Monte Negro, Singapore, Sri Lanka, United Kingdom, and United States.
VITATOPS aims to recruit and follow up 8,000 patients between 2000 and 2006, and provide a reliable estimate of the safety and effectiveness of dietary supplementation with folic acid, vitamin B12, and vitamin B6 in reducing recurrent serious vascular events, dementia and depression among a wide range of patients with stroke and TIA.
Please refer to this study by its ClinicalTrials.gov identifier: NCT00097669
Show 111 Study Locations
|Principal Investigator:||Graeme Hankey, MBBS/MD||Royal Perth Hospital / University of Western Australia|
|Study Director:||Ross Baker, MBBS/BMedSc||Royal Perth Hospital|
|Study Director:||John Eikelboom, MBBS/FRACP||Royal Perth Hospital|
|Study Director:||Konrad Jamrozik, MBBS||The University of Queensland|
|Study Director:||Frank van Bockxmeer, BSc/PhD||Royal Perth Hospital|
|Study Director:||Siobhan Hickling, BSc/MPH||The University of Western Australia|
|Study Director:||Anna Gelavis, BPharm||Royal Perth Hospital|