Table 1.

Timetable of patient enrollment and intervention and data collection.

Study schedule	Patient information and inclusion	Intervention period
Visit 1	0	1
Time	≥12h before procedure	0
Patient information	✓a	—b
Informed consent	✓	—
Baseline characteristics: age, gender, CVRFc, etc	✓	—
BPd recordings	—	✓
Primary outcome	—	✓
Secondary outcome	—	✓
Safety outcome	—	✓

^aThis item is included.

^bThis item is not included.

^cCVRF: cardiovascular risk factor.

^dBP: blood pressure.