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N/A N=8,164 Randomized Quadruple-blind Prevention

VITATOPS: A Study of VITAmins TO Prevent Stroke

Stroke · Transient Ischemic Attack

Enrolled (actual)
8,164
Serious AEs
0.0%
Results posted
Sep 2020
Primary outcome: Primary: Non-fatal Stroke, Non-fatal Myocardial Infarction or Death Due to Vascular Causes — 616; 678 Participants — p=0.05

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Active VITATOPS Tablet (folic acid 2mg, B6 25mg , B12 500ug) or placebo (Drug); Placebo (Other)
Age
Pediatric, Adult, Older Adult
Sex
All
Sponsor
VITATOPS
Primary completion
Jun 2009

Outcome Measures

OutcomeResultp-value
PRIMARY
Non-fatal Stroke, Non-fatal Myocardial Infarction or Death Due to Vascular Causes
616; 678 0.05

Summary

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.

Eligibility Criteria

Inclusion Criteria

  • Patients presenting within seven months of stroke (ischemic or hemorrhagic) or TIA
  • Agree to take study medication
  • Be geographically accessible for follow-up
  • Provide written informed consent

Exclusion Criteria

  • Taking folic acid or B6 on medical advice
  • Use of vitamin supplements containing folate, B6 or B12 (unless patient agrees to take study medication instead of the vitamin supplements which they usually take)
  • Taking Methotrexate for any reason
  • Pregnancy or women of child-bearing potential who are at risk of pregnancy
  • Limited life expectancy
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00097669). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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