02111nas a2200217 4500000000100000008004100001100001500042700001100057700001500068700001700083700001600100700001000116700001300126700001900139245011100158250001500269300000800284490000700292520154500299020004901844 2013 d1 aLatimer J.1 aDay R.1 aHancock M.1 aMcLachlan A.1 aWilliams C.1 aLin C1 aMaher C.1 aBillot Laurent00aPACE--the first placebo controlled trial of paracetamol for acute low back pain: statistical analysis plan a2013/08/14 a2480 v143 a
BACKGROUND: Paracetamol (acetaminophen) is recommended in most clinical practice guidelines as the first choice of treatment for low back pain, however there is limited evidence to support this recommendation. The PACE trial is the first placebo controlled trial of paracetamol for acute low back pain. This article describes the statistical analysis plan. RESULTS: PACE is a randomized double dummy placebo controlled trial that investigates and compares the effect of paracetamol taken in two regimens for the treatment of low back pain. The protocol has been published. The analysis plan was completed blind to study group and finalized prior to initiation of analyses. All data collected as part of the trial were reviewed, without stratification by group, and classified by baseline characteristics, process of care and trial outcomes. Trial outcomes were classified as primary and secondary outcomes. Appropriate descriptive statistics and statistical testing of between-group differences, where relevant, have been planned and described. CONCLUSIONS: A standard analysis plan was developed for the results of the PACE study. This plan comprehensively describes the data captured and pre-determined statistical tests of relevant outcome measures. The plan demonstrates transparent and verifiable use of the data collected. This a priori plan will be followed to ensure rigorous standards of data analysis are strictly adhered to. TRIAL REGISTRATION: Australia and New Zealand Clinical Trials Registry ACTRN12609000966291.
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