Table 1.
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 | √ |