hypertension
Conditions
Interventions
Experimental group:Qinggan Yishen Qufeng Formula+Western medicine
Control group:Western medicine
Sponsors
Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of TCM
Eligibility
Sex/Gender
All
Age
20 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Patients with blood pressure=140/90mmHg for =3 times on separate days, or currently with on antihypertensive therapy; 2. Patients whose total cardiovascular risk are high or very high risk according to hypertensive guideline released by European society of hypertension: (1) Grade 1 hypertension (SBP 140–159 and/or DBP 90–99mmHg) and = 3risk factors; (2) Grade 2 hypertension (SBP 160–179 and/or DBP 100–109mmHg) and =2 risk factors; (3) Grade 3 hypertension (SBP=180 and/or DBP=110mmHg); 3.Willing to participate with informed consent signed.
Exclusion criteria
Exclusion criteria: 1 Secondary hypertension, confirmed or suspected; 2 Failure of ambulatory blood pressure monitoring: effective reading 2 times normal), renal insufficiency (serum creatinine clearance < 30ml/min); 4 Pregnant or breastfeeding (female); 5 Combined with other diseases not suitable for the test, such as acute infectious diseases, chronic mental diseases, tumors, etc.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in 24-hour ambulatory blood pressure mean systolic blood pressure (24-hour SBP); | — |
Secondary
| Measure | Time frame |
|---|---|
| Changes in home blood pressure;Changes in clinic blood pressure;Changes in 24-hour mean diastolic blood pressure (24h DBP), daytime systolic blood pressure (SBP), and nighttime systolic blood pressure (DBP); | — |
Countries
China
Contacts
Public ContactYang Yawei
Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of TCM
Outcome results
None listed