None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients who have decided to participate in the SVKHCT-MA-23-02 study. 2) Patients who have consented to 24-hour ABPM. 3) Patients who have voluntarily provided written informed consent to participate in this observational sub-study.
Exclusion criteria
Exclusion criteria: 1) Patients currently participating in other interventional studies. 2) Patients deemed unsuitable for participation by the investigator for any other reason.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change from baseline in mean 24-hour systolic blood pressure (SBP) at 12 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Change in the proportion of dipper/non-dipper patients from baseline at 12 months;Change from baseline in mean Morning Blood Pressure Surge (MBPS) at 12 months;Change from baseline in mean nighttime/daytime pulse pressure at 12 months;24-hour systolic/diastolic blood pressure control rate at 12 months compared to baseline;Daytime and nighttime systolic/diastolic blood pressure control rates at 12 months compared to baseline;Change from baseline in mean 24-hour diastolic blood pressure (DBP) at 12 months;Change from baseline in mean nighttime systolic/diastolic blood pressure at 12 months;Change from baseline in mean daytime systolic/diastolic blood pressure at 12 months | — |
Countries
Korea, Republic of
Contacts
Seoul National University Bundang Hospital