Essential Hypertension
Conditions
Interventions
Control Group:Placebo
Experimental Group:XLF
Sponsors
Beijing Hospital of Traditional Chinese Medicine
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: (1) Meet the diagnostic criteria for essential hypertension and there is no limit to grade 1 2 and 3 hypertension. (2) Meet the evaluation criteria of high salt intake that is people with salt intake > 10g/d; (3) meet the diagnostic criteria for phlegm turbidity syndrome; (4) Age 18-80 years old gender is not limited; (5) Patients and their families agree to participate in the trial and sign an informed consent form.
Exclusion criteria
Exclusion criteria: (1) Patients with uncontrolled severe hypertension or hypertensive emergencies and subemergencies. (2) Patients with secondary hypertension. (3) Patients with acute coronary syndrome or acute heart failure/acute exacerbation of chronic heart failure valvular heart disease with obvious hemodynamic changes and severe malignant arrhythmias or patients with cardiomyopathy pulmonary heart disease viral myocarditis and congenital heart disease; (4) Patients with hyperthyroidism malignant tumors hematologic diseases and acute infections; (5) Women who are pregnant or lactating; (6) Abnormal liver function (ALT or AST higher than the upper limit of normal) abnormal renal function (Cr>3mg/dl); (7) Patients with mental illness or cognitive and memory impairments; (8) Patients who are unable to cooperate with the completion of TCM-related symptoms tongue and pulse information collection and questionnaire surveys (9) Any other condition that the investigator considers the patient to be unsuitable to participate in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| BP qualified rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| Target organ damage;BP effective rate;TCM syndrome score;TCMSS effective rate; | — |
Countries
China
Contacts
Public ContactLiu Hongxu
Beijing Hospital of Traditional Chinese Medicine
Outcome results
None listed