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Clinical Observation on the Efficacy of Shexiang Baoxin Pill Combined with Standardized Anti-Heart Failure Therapy in the Treatment of Ischemic Cardiomyopathy

Clinical Observation on the Efficacy of Shexiang Baoxin Pill Combined with Standardized Anti-Heart Failure Therapy in the Treatment of Ischemic Cardiomyopathy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500108457
Enrollment
Unknown
Registered
2025-09-01
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

ischemic cardiomyopathy

Interventions

Exposure Group (Shexiang Baoxin Pill plus standardized anti-heart failure therapy) :None
Non-exposure Group (standardized anti-heart failure therapy):None

Sponsors

The Second Affiliated Hospital of Hainan Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years, with no gender restriction; 2. Diagnosed with significant stenosis (>= 75%) in at least one coronary artery by coronary angiography or coronary CTA, or with a history of Percutaneous Coronary Intervention (PCI) or Coronary Artery Bypass Grafting (CABG), and receiving secondary prevention therapy for coronary heart disease; 3. Presence of heart failure symptoms or signs such as chest tightness, dyspnea, or edema, with NT-proBNP > 125ng/L; 4. New York Heart Association (NYHA) functional class II–IV; 5. Patients voluntarily sign the informed consent form for this study.

Exclusion criteria

Exclusion criteria: 1. Patients with malignant hypertension; 2. Patients with severe arrhythmia, valvular heart disease, or cardiogenic shock; 3. Patients with moderate to severe hepatic or renal dysfunction, complicated by severe metabolic diseases, hematological diseases, or malignant tumors; 4. Patients with excessive missing medical records and biochemical index data; 5. Pregnant women, lactating women, or women of childbearing age with fertility requirements; 6. Patients allergic to the drugs involved in this study; 7. Patients deemed by researchers to be unsuitable for enrollment due to other factors.

Design outcomes

Primary

MeasureTime frame
Left Ventricular Ejection Fraction;

Secondary

MeasureTime frame
N-terminal pro-brain natriuretic peptide;Kansas City Cardiomyopathy Questionnaire;6-Minute Walk Distance;

Countries

China

Contacts

Public ContactChen Yuewu

The Second Affiliated Hospital of Hainan Medical University

eyuewu@hainmc.edu.cn+86 135 1808 5982

Outcome results

None listed

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