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Bleeding events were categorized into major and minor events.
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The bleeding events were recorded throughout the observation period.
When bleeding events were analysed as ordinal data (no bleed, minor bleed, major bleed)[19], significantly increased rates were seen in the triple therapy group (p<0.01).
Adverse bleeding events were also examined.
Bleeding events were recorded for 28 days.
Five major bleeding events were noted.
Major bleeding events and clinically relevant non-major bleeding events were defined according to accepted guidelines.
Ischemic and bleeding events were recorded during the trial.
The total bleeding events, including both major and minor bleeding events, were recorded throughout the observation period.
Bleeding events occurred at a similar rate in each group and no major bleeding events were seen in any group.
All major bleeding events and clinically relevant non-major bleeding events were adjudicated according to the standardised model of bleeding definitions 25 (box 1).
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