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Observation on the Clinical Efficacy of Shen'ge Powder in Treating Heart Failure in Patients with Dilated Cardiomyopathy of Heart-Kidney Yang Deficiency Type

Observation on the Clinical Efficacy of Shen'ge Powder in Treating Heart Failure in Patients with Dilated Cardiomyopathy of Heart-Kidney Yang Deficiency Type

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096005
Enrollment
Unknown
Registered
2025-01-16
Start date
2025-01-23
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Dilated cardiomyopathy

Interventions

Control group:Conventional Western medicine treatment group
Treatment group:Shen'ge Powder Combined with Conventional Western Medicine

Sponsors

Shanghai Fifth Peoople's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic criteria of Western medicine and traditional Chinese medicine syndrome diagnosis of dilated cardiomyopathy; (2) Cardiac function grade (NYHA) grade II-IV; (3) Age 35-80 years; (4) During the test, other traditional Chinese medicines or intravenous preparations of traditional Chinese medicine were not used at the same time; (5) Those who agree to participate in clinical trial observation and can persist in completing treatment and observation index testing; (6) Signed and dated informed consent.

Exclusion criteria

Exclusion criteria: (1) History of acute myocardial infarction, coronary stent implantation, coronary artery bypass grafting; Patients with severe arrhythmias, pulmonary embolism, shock and other life-threatening diseases such as ventricular tachycardia, second-degree and type II atrioventricular block; (2) Patients with bronchial asthma, chronic bronchitis, cor pulmonale, and chronic obstructive pulmonary disease; (2) Patients with severe liver and kidney insufficiency, hyperthyroidism, hypothyroidism, anemia and electrolyte imbalance; (3) Pregnant or lactating women; (4) Patients with serious internal diseases, such as respiratory system, digestive system, blood system, immune system or diseases that may pose serious danger to patients; (5) Allergies or allergies to common drugs; (6) Those who have recently participated in other clinical research studies of traditional Chinese medicine or those who are currently taking other traditional Chinese medicines regularly and are unwilling to stop taking them; (7) Patients with mental illness or poor compliance with traditional Chinese medicine treatment.

Design outcomes

Primary

MeasureTime frame
Clinical efficacy and improvement of cardiac function;

Secondary

MeasureTime frame
Echocardiography;NT-proBNP;Evaluation of the efficacy of TCM syndrome;TGF-ß1;Lee's heart failure score;

Countries

China

Contacts

Public ContactZhou Chang

Shanghai Fifth Peoople's Hospital

zhouchang_cc@163.com+86 19821251279

Outcome results

None listed

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