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A randomized, double-blind, placebo-controlled clinical study on the treatment of hypertension(grade 1,low to medium risk) with Qingda granules

A randomized, double-blind, placebo-controlled clinical study on the treatment of hypertension(grade 1,low to medium risk) with Qingda granules

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000123
Enrollment
Unknown
Registered
2024-07-10
Start date
2024-08-01
Completion date
Unknown
Last updated
2024-07-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Essential hypertension

Interventions

Negative control group:Qingda particle simulator
Experimental group:Qingda granules

Sponsors

Long Linzi
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients met the diagnostic criteria of hypertension level 1 according to the unified office blood pressure measurement, and the risk stratification was low and intermediate risk (according to the Chinese Guidelines for the prevention and treatment of Hypertension, revised edition 2018) Not taking antihypertensive drugs within one month TCM syndrome differentiation conforms to the liver-Yang hyperthyroidism syndrome Age between 20 and 75 years old (including boundary values) Sign the informed consent form

Exclusion criteria

Exclusion criteria: Patients with obvious liver and kidney diseases or glutamic-pyruvic transaminase and glutamic-oxalacetic transaminase are 1.5 times higher than normal value, and creatinine and urea nitrogen are 2 times higher than normal value Have the following diseases: Acute myocardial infarction, cerebrovascular accident, transient ischemic attack, large aneurysm or dissecting aneurysm, unstable angina pectoris, heart failure history of Grade II-IV (NYHA scale), atrioventricular block of grade II and above, sick sinus syndrome, bradycardia (heart rate < < 50 times/min) or patients with malignant or potentially malignant arrhythmias such as atrial fibrillation, serious mental diseases, diseases of the hematopoietic system, malignant tumors and other major diseases Secondary hypertension, including but not limited to the following diseases: unilateral or double renal arteries, polycystic kidney disease, hyperaldosteronism, coarctation of the aorta, Cushing's syndrome, pheochromocytoma Circadian rhythm reversal or irregular sleep pattern pregnancy, lactation or family planning within 6 months Have participated in or are participating in other clinical investigators within the last three months Suspected or clear allergy to the study drug

Design outcomes

Primary

MeasureTime frame
Change from baseline in office systolic blood pressure after 4 weeks of treatment;

Secondary

MeasureTime frame
Ambulatory blood pressure control after 4 weeks of treatment;Vasoactive substances after 4 weeks of treatment;Changes of total score of liver-yang hyperactivity syndrome after 4 weeks of treatment;Change in diastolic blood pressure from baseline after 4 weeks of treatment;

Countries

China

Contacts

Public ContactLong Linzi

Xiyuan Hospital of China Academy of Chinese Medical Sciences

qixiang830803@163.com15801152337

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026