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A non-significant lower odds of having a poor clinical outcome was also found in the intervention, relative to control group of 4% (odds ratio 0.96; 95% CI 0.56-2.07) and higher odds of having poor outcome of 44% (odds ratio 1.44 95% CI 0.61-3.41) during both active and post-intervention period respectively. Similarly, a non-significant lower odds of parenchymal haematoma was also found for the intervention group during the both active- (odds ratio 0.53; 95% CI 0.21-1.32) and post-intervention period (odds ratio 0.96; 95% CI 0.36-2.52).
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