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Clinical Study on Regulating Myocardial Energy Metabolism of Qianyang Yuying Granules to Improve Hypertensive Cardiopathy in the Elderly Patients

Clinical Study on Regulating Myocardial Energy Metabolism of Qianyang Yuying Granules to Improve Hypertensive Cardiopathy in the Elderly Patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069738
Enrollment
Unknown
Registered
2023-03-24
Start date
2023-03-24
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Hypertensive Cardiopathy

Interventions

Experimental group:Western medicine standard treatment combined with Qianyang Yuyin Granules

Sponsors

Affiliated Hospital of Nanjing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. In line with TCM syndrome of yin deficiency and yang hyperactivity; 2. Aged 60 to 80 years; 3. Patients with primary hypertension of grade 1-2 ; 4. Left Ventricular hypertrophy was consistent with ECG Sokolow-lyon voltage >3.8mV or Cornell product >244mV·ms, or echocardiographic Left Ventricular Mass Index (LVMI): male =115g/m2, female =95g/m2; 5. ARB or CCB drugs can reduce blood pressure to meet the requirements, systolic blood pressure (SBP) =140mmHg and diastolic blood pressure (DBP) =90mmHg; 6. Sign the informed consent for entry into the study.

Exclusion criteria

Exclusion criteria: 1. Secondary hypertension; 2. Complicated with serious cardiovascular target organ complications, such as acute myocardial infarction, stroke, grade IV heart failure, malignant arrhythmia, etc.; 3. Other Chinese and Western drugs have been used to treat essential hypertension; 4. Patients with definite contraindications to the use of ARB or CCB drugs; 5. Patients with significantly abnormal liver function; 6. Unable to give full informed consent due to intellectual or behavioral disabilities; 7. Suspected or confirmed history of alcohol and drug abuse; 8. Other diseases that reduce the possibility of enrollment or complicate enrollment, such as frequent changes in the working environment, are likely to cause loss of follow-up according to the judgment of the researcher; 9. Allergies, such as allergies to two or more drugs or foods; or known allergies to the ingredients of the drug; 10. Patients who are participating in clinical trials of other drugs.

Design outcomes

Primary

MeasureTime frame
Diastolic ventricular septal thickness;Left ventricular posterior wall thickness (LVPWd);Left ventricular end-diastolic diameter (LVIDd);Early diastolic peak (E);Late diastolic peak;Left ventricular ejection fraction;E/e’;E/A;Left ventricular mass;Left ventricular mass index;

Secondary

MeasureTime frame
tumor necrosis factor-a ;intercellular adhesion molecule-1;vascular cell adhesion molecule-1;monocyte chemotactic protein 1 ;Interleukin-1ß;Interleukin-6;8-hydroxydeoxyguanosine;reactive oxygen species ;superoxide dismutase ;glutathione peroxidase;malondialdehyde ;

Countries

China

Contacts

Public ContactFangYuan

Affiliated Hospital of Nanjing University of Chinese Medicine

QueenieFang@outlook.com+8618951755242

Outcome results

None listed

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