Skip to content

The efficacy assessment of the curative efficacy of the coronary arterial microvascular disease in the coronary arteries: random dual-blind placebo control test

The efficacy assessment of the curative efficacy of the coronary arterial microvascular disease in the coronary arteries: random dual-blind placebo control test

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088473
Enrollment
Unknown
Registered
2024-08-20
Start date
2024-03-06
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Coronary arterial microvascular disease

Interventions

Test group:After the meal, orally Guanxinning tablet, 4 tablets at a time, 3 times a day.
Control group:After the meal, orally Guanxinning placebo, 4 tablets at a time, 3 times a day.

Sponsors

Run Run Shaw Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) 18-80 years old; (2) Individuals exhibiting symptoms of exertional or resting angina; (3) Patients with ischemic electrocardiographic changes during angina attacks, or positive results in plate exercise tests, or transient and reversible local wall motion abnormalities or perfusion defects during stress single photon emission computed tomography (SPECT)/PET/cardiac magnetic resonance imaging (MRI)/echocardiography examinations, or other evidence of myocardial ischemia; (4) MFR<2.0 and/or MPRI<2.0 for cardiac magnetic resonance imaging (CMR); (5)Voluntarily participate in this study and sign an informed consent form. If the subject does not have the ability to read the informed consent form (such as illiterate subjects), a witness must witness the informed process and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Subcardiac coronary artery stenosis = 50%; (2) Thrombotic coronary artery disease; (3) Acute coronary syndrome (within 1 year) or within 12 months after percutaneous coronary intervention with complete revascularization; (4) Severe heart failure (EF3 times the upper limit of normal); (15) Renal insufficiency (eGFR<30ml/min/1.73m2); (16) Acute exacerbation or worsening of chronic diseases; (17) Expected survival period<1 year; (18) Vulnerable groups, including individuals with mental illness, cognitive impairment, critically ill patients, minors, pregnant women, etc. (19) Patients who have participated in other clinical trials within the past month. (20) Researchers believe that there are patients with other factors that are not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
Myocardial blood flow reserve;Myocardial perfusion reserve index;Hemoglobin;

Secondary

MeasureTime frame
High density lipoprotein;Low density lipoprotein;Total cholesterol;Triglyceride;Alanine aminotransferase;Aspartate transaminase;Alkaline phosphatase;Gamma glutamyltransferase;Total bilirubin ;Direct bilirubin;Serum creatinine;Glomerular filtration rate;Urea nitrogen;Lipoprotein A;Glycosylated hemoglobin;Homocysteine;C-reactive protein;Activated partial thromboplastin time;Prothrombin time;International standardized ratio;D-dimer;Natriuretic peptide;Troponin I;Red blood cell;White blood cell;Platelet;Bld ;Urinary white blood cells;Urine protein;Urinary ketone bodies;Urobilinogen;Urine pregnancy test;Fecal occult blood;Fecal white blood cells;Serum untargeted metabolomics;Seattle Angina Questionnaire;Electrocardiogram;Cardiac ultrasound;Incidence of major adverse cardiovascular events (MACE);

Countries

China

Contacts

Public ContactHuang he

Run Run Shaw Hospital, Zhejiang University School of Medicine

huanghell@zju.edu.cn+86 139 5808 5799

Outcome results

None listed

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