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Study on the innovative pathogenesis of dilated cardiomyopathy heart failure and its clinical identification and treatment scheme

Study on the innovative pathogenesis of dilated cardiomyopathy heart failure and its clinical identification and treatment scheme

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072903
Enrollment
Unknown
Registered
2023-06-27
Start date
2023-06-23
Completion date
Unknown
Last updated
2023-10-22

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

Conditions

Heart Disease

Interventions

Qishen granule optimization group:On the basis of standardized western medicine treatment, Qishen granule optimized prescription was given for 12 weeks.
Qishen granule original prescription group:On the basis of standardized western medicine treatment, Qishen granule optimized prescription and Qishen granule original prescription were given.
placebo group:On the basis of standardized Western medicine treatment, placebo granules are given.

Sponsors

The First Affiliated Hospital of Guangzhou University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria of chronic heart failure (see Appendix 1 for details); 2. Meet the diagnostic criteria of dilated heart disease (see Appendix 2 for details); 3. Meet the diagnostic criteria of heart failure syndrome of heart failure (note: the diagnostic criteria of heart failure syndrome are drawn up after pre-epidemiological investigation); 4. LVEF = 600 PG mL; 5. NYHAII-III grade; 6. Aged 18-80 years; 7. Volunteer to participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Acute stage of myocardial infarction; 2. Severe hepatic insufficiency (ALT > 100 U/L or AST > 100 U/L), severe renal insufficiency (glomerular filtration rate 5.5 mmol/L); 3. Blood diseases and malignant tumors; 4. Pregnant or lactating women; 5. Psychiatric patients; 6. Uncontrollable hypertension or diabetes; 7. People who are allergic to experimental drug ingredients; 8. Those who take experimental drugs, other traditional Chinese medicine or proprietary Chinese medicine within one month; 9. Those who are known to have adverse reactions to research drugs.

Design outcomes

Primary

MeasureTime frame
Left ventricular ejection fraction, LVEF;NT-proBNP;

Secondary

MeasureTime frame
Left ventricular end-diastolic diameter, LVEDD;Left ventricular end-systolic diameter, LVESD;interventricular septal thickness (IVST);LVPW, left ventricular posterior wall thickness;Left ventricular fractional shortening (FS);E/E’;E/A;TCM syndrome integral;ST2;NYHA cardiac function classification;Minnesota Heart failure quality of Life scale;Grading and quantification table of heart failure symptoms;6MWT, 6-minute walking test;

Countries

China

Contacts

Public ContactLi Rong

The First Affiliated Hospital of Guangzhou University of Chinese Medicine

lrhbs@126.com+86 137 9818 4933

Outcome results

None listed

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