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Side effect rates between allicin and control groups (intent-to-treat/per-protocol analysis). There was no statistical significance in side effect rates between the allicin group and control group for ITT analysis [5.90% (18/305) vs 9.53% (29/304), odds ratio = 0.61, 95% confidence interval: 0.32-1.16, P = 0.133]. CI: Confidence interval.
