Skip to content

Clinical study on the treatment of liver-yang-excessive hypertension combined with early renal damage with Pingtiao granules

Clinical study on the treatment of liver-yang-excessive hypertension combined with early renal damage with Pingtiao granules

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000280
Enrollment
Unknown
Registered
2024-08-21
Start date
2024-06-19
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Hypertension combined with early kidney damage

Interventions

control group:Treated with valsartan capsules
test group:Received valsartan capsules and Pingtiao granules

Sponsors

Guangzhou University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 79 Years

Inclusion criteria

Inclusion criteria: (1) Patients who meet the diagnostic criteria for hypertension and have a blood pressure classification of grade 1 or 2; (2) Those whose laboratory indicators meet the criteria for early renal damage; (3) Those who meet the diagnostic criteria of Chinese medicine symptoms of liver-yang over-excessive syndrome; (4) Patients aged 18-79 years old; (5) Patients who were informed and agreed to participate in the study.

Exclusion criteria

Exclusion criteria: (1) Patients with secondary hypertension, hypertensive emergencies and hypertensive crises; (2) Patients with primary renal disease and chronic renal insufficiency caused by other diseases; (3) Serious heart and brain diseases, such as myocardial infarction, angina pectoris, heart failure, patients with serious valvular diseases, cerebral infarction, cerebral hemorrhage patients within the last 3 months; (4) Patients with major diseases combined with severe target organ damage, malignant tumors, severe infections, immune dysfunction and so on; (5) Obvious contraindication or intolerance to the test drug; (6) Allergic body and allergic to multiple drugs; (7) Nursing and pregnant women; (8) Those who have recently taken traditional Chinese medicine that affects the identification and typing of evidence; (9) People with mental and cognitive disorders and poor compliance who cannot cooperate with the follow-up; (10) Participants in other studies at the same time.

Design outcomes

Primary

MeasureTime frame
Um ALB;Coefficient of variation;Average blood pressure;ß2-MG;Cys C;

Secondary

MeasureTime frame
Chinese Medicine Evidence Rating Scale;Salt sensitivity risk;Dynamic atherosclerosis index;Blood pressure circadian rhythm;Morning blood pressure surge;

Countries

China

Contacts

Public ContactCui Meng-Yao ,Jin Li-Li

Guangzhou University of Chinese Medicine

760380849@qq.com13969612239

Outcome results

None listed

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