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A novel non wire microcirculation resistance index (AMR) based on quantitative blood flow fraction (QFR) for postoperative prognosis evaluation and traditional Chinese medicine intervention of coronary artery intervention therapy

A novel non wire microcirculation resistance index (AMR) based on quantitative blood flow fraction (QFR) for postoperative prognosis evaluation and traditional Chinese medicine intervention of coronary artery intervention therapy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400090721
Enrollment
Unknown
Registered
2024-10-12
Start date
2024-12-01
Completion date
Unknown
Last updated
2024-10-21

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

Conditions

Coronary artery disease

Interventions

Group of patients treated with coronary intervention-Normal AMR(Part I):NA
Nomal microcirculation resistance group-High AMR(Part I):NA
Normal microcirculatory resistance group(Part II):On the basis of conventional treatment, add 2 capsules of Musk Baoxin Pill orally for 3-6 months
Elevated microcirculation resistance group(Part II):On the basis of conventional treatment, add 2 capsules of Musk Baoxin Pill orally for 3-6 months

Sponsors

Shaoxing Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Part I: Retrospective Trial: Select PCI patients who underwent coronary intervention treatment in our hospital from January 2021 to June 2022, and screen suitable patients for enrollment. Inclusion criteria: 1. Age over 18 years old; 2.DSA images are clear and complete, capable of completing QFR and AMR detection; 3.The follow-up data is basically complete; Part II: Prospective Study The PCI patients who underwent coronary intervention in our hospital from Dec 2024 to Dec 2025 were selected, and suitable patients were selected for enrollment. Inclusion Criteria: 1. Be at least 18 years old; 2.Stable or unstable angina, or acute myocardial infarction, or evidenced asymptomatic myocardial ischemia; 3.Able to understand the trial design and sign a written informed consent form

Exclusion criteria

Exclusion criteria: Part I: Retrospective Trial: Exclusion criteria: 1. Cardiogenic shock or severe heart failure (NYHA = III); 2.Severe impairment of renal function: dialysis status or creatinine clearance rate GFR<45 mL/kg/1.73 m2 (calculated using the Cockcroft Gault formula); 3.Known malignant tumors and severe hematological disorders; Part II: Prospective Studies Exclusion criteria: 1.Cardiogenic shock or severe heart failure (NYHA = III); 2.Severe impairment of renal function: dialysis status or creatinine clearance rate GFR<45 mL/kg/1.73 m2 (calculated using the Cockcroft Gault formula); 3.Known malignant tumors and severe hematological disorders; 4.Life expectancy is less than 1 year; 5.Preparing pregnant women within one year;

Design outcomes

Primary

MeasureTime frame
Cardiovascular Death (Part I);Heart Failure (Part I);Malignant arrhythmias (Part I); microcirculation resistance index (AMR) ;

Secondary

MeasureTime frame
Cardiovascular Death (Part II);Heart Failure (Part II);Malignant arrhythmias (Part II);

Countries

China

Contacts

Public ContactJianyao Shen

Department of Cardiology, Shaoxing Central Hospital (The Central Affiliated Hospital, Shaoxing University), Shaoxing 312030, Zhejiang,China

jianyao_s@163.com+86 137 3526 5055

Outcome results

None listed

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