American Heart Journal
Volume 154, Issue 5 , Pages 815-823.e6 , November 2007

Study of the effectiveness of additional reductions in cholesterol and homocysteine (SEARCH): Characteristics of a randomized trial among 12064 myocardial infarction survivors

  • SEARCH Study Collaborative Group

Received 13 October 2006 ,Accepted 22 June 2007.

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    Eligibility for SEARCH. *The upper age limit was raised from 75 to 80 in a protocol amendment in June 2000.

    Eligibility for SEARCH. *The upper age limit was raised from 75 to 80 in a protocol amendment in June 2000.

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    Trial profile.

    Trial profile.

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    Relation between the proportional reduction in vascular event rate and mean absolute LDL-C difference. Gray square represents summary result for MVEs from Cholesterol Treatment Trialists' (CTT) collab

    Relation between the proportional reduction in vascular event rate and mean absolute LDL-C difference. Gray square represents summary result for MVEs from Cholesterol Treatment Trialists' (CTT) collaborative meta-analysis of effect of 1 mmol/L LDL-C reduction in randomized trials of statin versus no statin.3 Sloping line plotted through zero and CTT result. Solid squares represent individual trials comparing more versus less intensive statin therapy, with data derived from published meta-analysis.10 (Directly comparable outcome is not available for these trials, so endpoint of “CHD death or MI” is plotted.) Average achieved LDL difference for A-to-Z is based on aggregate of achieved differences during month 1, months 2 to 4, and thereafter.6 Open square represents projected result for SEARCH, based on primary outcome of MVE and estimated average LDL-C difference of 0.4 mmol/L between intensive and standard statin groups. The area of each square is proportional to the amount of statistical information in trial or meta-analysis. Vertical lines are 95% CIs.

 The study is funded by a grant to the University of Oxford, Oxford, United Kingdom, from Merck & Co, Inc, Whitehouse Station, NJ. It has, however, been designed and conducted, and will be analyzed and interpreted by the Clinical Trial Service Unit independently of this source of support.

☆☆ The Clinical Trial Service Unit has a staff policy of not accepting honoraria or other payments from the pharmaceutical industry, except for reimbursement of costs to participate in scientific meetings.

PII: S0002-8703(07)00533-9

doi: 10.1016/j.ahj.2007.06.034

American Heart Journal
Volume 154, Issue 5 , Pages 815-823.e6 , November 2007