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. 2020 Jul 5;10(7):e036061. doi: 10.1136/bmjopen-2019-036061

Table 1.

Schedule for data collection; outcome measures per visits

Items Phase Ι:
screening
Phase II:
baseline
Phase III:
1 month
Phase Ⅳ:
3 months
Phase Ⅴ:
6 months
Inclusion/exclusion criteria
Diagnostic index
Signed informed consent
Randomisation and allocation
Safety index
General clinical information
Primary outcomes
Secondary outcomes
Other indicators
Recurrent cardiovascular events
Adherence
Adverse events
Summary at the end of the study