Hypertension
Conditions
Keywords
Gastrodia and Uncaria, Stage one Hypertension, Liver yang hyperactivity
Brief summary
Gastrodia and Uncaria Recipe is a well-known effective prescription in Traditional Chinese Medicine (TCM) to treat hypertension of liver yang hyperactivity type, which manifests symptom of headache or dizziness. However, it lacks consolidated evidence by multi-center randomized controlled trials. The hypothesis of this study is that Gastrodia and Uncaria granule may have significant anti-hypertensive effect on patients with stage-one hypertension and liver-yang hyperactivity syndrome than placebo. This study is a randomized, controlled, multi-center, double-blind clinical trial. This study aims to recruit 500 hypertension patients who 1) are untreated or taking anti-hypertensive medicine for at least two weeks and 2) have an office systolic blood pressure of 140-159 mmHg, an office diastolic blood pressure of \<100 mmHg, and a 24-hour ambulatory mean systolic blood pressure of \>=130 mmHg. The patients will be stratified according to center, sex, and the TCM type of liver yang hyperactivity/ liver yang non-hyperactivity, and are then randomly assigned to the treatment of Gastrodia and Uncaria granules or placebo for 2 months. The blood pressure lowering effect is evaluated by 24-hour ambulatory systolic blood pressure (primary outcome) / diastolic blood pressure, as well as by home and office blood pressures.
Interventions
DRUGGastrodia and Uncaria granule
Patients allocated to the intervention group take 10g of Gastrodia and Uncaria granule each time, twice per day, and for two months.
DRUGPlacebo of Gastrodia and Uncaria granule
Patients allocated to the control group take 10g of placebo of Gastrodia and Uncaria granule each time, twice per day, and for two months. The placebo has similar appearance and smell to genuine drug but has no effective anti-hypertensive agents.
Sponsors
Ruijin Hospital
Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
Shanghai Institute of Hypertension
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
1. Male and female sex, aged 18-80 years. 2. Not taking anti-hypertensive drugs for at least two weeks, or taking anti-hypertensive drugs for more than two weeks. 3. Office blood pressure averages of three consecutive readings per visit, at two screening visits all meet the limits: systolic blood pressure ranges from 140 to 159 mmHg, and diastolic blood pressure \<100 mmHg. 4. 24h ambulatory mean systolic blood pressure \>= 130mmHg. 5. Agreed to participant, able to join follow-up and to come to hospital at each visit. 6. Signed informed consent.
Exclusion criteria
1. Secondary hypertension, confirmed or suspected. 2. Failed at ambulatory blood pressure monitoring: effective reading \< 70%, or the number of awakening BP reading \<20, or sleep time BP reading \<7. 3. Taking drugs that must be used for other diseases but have a potential effect on blood pressure, such as males taking alpha blockers for prostatic hypertrophy. 4. Having the onset of cardiovascular and cerebrovascular diseases such as stroke, myocardial infarction or heart failure within 6 months. 5. Having a history of atrial fibrillation or frequent arrhythmia. 6. Having abnormal lab test results: liver function (ALT, AST, TBL) ≥ 2 times the upper normal limit, or serum creatinine ≥ 176umol/L, or serum potassium ≥ 5.5mmol/L. 7. Pregnant or breastfeeding (for females). 8. Complicating other diseases that are not suitable for the trial, such as thyroid disease with active medication, acute infectious diseases, chronic mental illness, and tumors. 9. Possible poor compliance with the research process.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in 24-hour ambulatory systolic blood pressure | 8 weeks | The difference of change of 24h ambulatory systolic blood pressure after 8-week treatment between treatment and control group |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in office blood pressure | 4 and 8 weeks | The difference of change of office systolic and diastolic blood pressure between treatment and control group |
| Change in 24-hour ambulatory systolic blood pressure by stratum | 8 weeks | The difference of change of 24h ambulatory systolic blood pressure after 8-week treatment between liver yang hyperactivity and liver yang non-hyperactivity stratum |
| Change in 24-hour ambulatory diastolic blood pressure, daytime and nighttime blood pressure | 8 weeks | The difference of blood pressure change of 24-hour mean ambulatory diastolic, daytime and nighttime systolic and diastolic between treatment and control group. |
| Change in home blood pressure | 8 weeks | Difference of change of home systolic and diastolic blood pressure after 8-week treatment between treatment and control group. |
Countries
China
Outcome results
None listed