Skip to content

Effect of Shexiang Baoxin Pill (MUSKARDIA) on Cardiac Function in Patients with Coronary Heart Disease and Heart Failure with Preserved Ejection Fraction: The Motivation Randomized Controlled Trial

Effect of Shexiang Baoxin Pill (MUSKARDIA) on Cardiac Function in Patients with Coronary Heart Disease and Heart Failure with Preserved Ejection Fraction: The Motivation Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097408
Enrollment
Unknown
Registered
2025-02-19
Start date
2025-03-01
Completion date
Unknown
Last updated
2025-02-24

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

Conditions

Heart failure

Interventions

Standard-care group (Standard treatment without MUSKARDIA):None
MUSKARDIA group (Standard treatment augmented with MUSKARDIA):Medication (MUSKARDIA)

Sponsors

The First Affiliated Hospital of University of Science and Technology of China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.Adults aged between 18 and 85 years; 2.Confirmed diagnosis of coronary heart disease via coronary angiography or computed tomography angiography (CTA); 3.Diagnosed with heart failure according to the criteria outlined in the "2024 Chinese Guidelines for the Diagnosis and Treatment of Heart Failure," with a left ventricular ejection fraction (LVEF) greater than 45%; 4.New York Heart Association (NYHA) functional class II to IV; 5.N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels exceeding 600 pg/mL; for patients with concomitant atrial fibrillation, NT-proBNP must exceed 900 pg/mL; 6.Provision of signed informed consent.

Exclusion criteria

Exclusion criteria: 1.Heart failure caused by non-cardiac origins such as valvular heart disease, congenital heart disease, pericardial disease, etc.; 2.Hospitalization for heart failure within the past 4 weeks; 3.Admission or cardiac surgery due to acute coronary syndrome within the past 4 weeks; 4.Coronary artery stenosis of less than 50% as shown by coronary angiography or CTA; 5.Uncontrolled hypertension (systolic blood pressure >=180 mmHg or diastolic blood pressure >=110 mmHg); 6.Severe hepatic, renal, or hematological disorders; 7.Pregnant or breastfeeding women; 8.Current use of MUSKARDIA or known allergy to it; 9.Uncontrolled psychiatric conditions or other systemic diseases; 10.Receipt of other investigational drug treatments within 30 days prior to randomization; 11.Inability to provide written informed consent.

Design outcomes

Primary

MeasureTime frame
NT-proBNP;

Secondary

MeasureTime frame
Kansas City Cardiomyopathy Questionnaire (KCCQ) score;Echocardiographic indicators;Heart failure hospitalization;Cardiovascular mortality;

Countries

China

Contacts

Public ContactChen Kangyu

The First Affiliated Hospital of University of Science and Technology of China

ahslyycky@126.com+86 180 5600 5099

Outcome results

None listed

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