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Evaluate the Efficacy and Safety of MUSK Pill on Coronary Microvascular Dysfunction

A Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Shexiang Baoxin Pill on Coronary Microvascular Dysfunction

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04984954
Enrollment
264
Registered
2021-08-02
Start date
2021-01-28
Completion date
2024-06-30
Last updated
2021-08-02

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

Conditions

Angina Pectoris, Coronary Heart Disease, Non Obstructive Coronary Artery Disease, X Syndrome, Angina

Keywords

Shexiang Baoxin Pill, Musk pill, Patients with coronary microvascular dysfunction

Brief summary

Objective to evaluate the effect of Shexiang Baoxin Pill on myocardial ischemia in patients with coronary microvascular dysfunction (non obstructive coronary heart disease) through a randomized, double-blind, placebo-controlled clinical multicenter study.At the same time, the effects of exercise tolerance and quality of life were also observed.

Interventions

DRUGMUSK pill

This is a multicenter, randomized, double-blind, placebo-controlled clinical trial. Patients were treated with the trial drug or placebo in a 1:1 ratio. The experimental group was treated with MUSK pill (4 pills / day, 3 times / day) on the basis of conventional treatment until the end of follow-up

Sponsors

Shanghai Hutchison Pharmaceuticals Limited
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Intervention model description

1:1 stratified block random grouping according to the center

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Patients aged 18-80, male or female; 2. Selective coronary angiography or coronary CTA showed that the diameter of coronary artery ≥ 2.5mm, the degree of stenosis \< 50%, without myocardial bridge; 3. They were able to perform treadmill exercise, and the treadmill test (EET) was positive; 4. Angina pectoris was found; 5. Patients are willing to follow up and sign informed consent; All the above criteria should be met.

Exclusion criteria

1. Coronary heart disease complicated with hypertrophic cardiomyopathy; 2. There was a history of AMI, PCI and CABG, and myocardial bridge was found by angiography or CTA; 3. Patients with severe medical diseases (liver, kidney, hematopoietic system and other serious primary diseases, etc.); 4. Mental disorders and mental diseases; 5. Patients with pulmonary failure and NYHA heart function grade III-IV, unable to carry out exercise test; 6. Contraindications of Shexiang Baoxin Pill: forbidden for pregnant women; 7. Those who have known history of allergy to Shexiang Baoxin Pills; 8. Recently, the patient has taken Shexiang Baoxin Pill and other anti ischemic traditional Chinese medicine regularly, or it contains borneol, toad venom and other ingredients in Shexiang Baoxin Pill; 9. Combined with frequent ventricular premature beats, ventricular tachycardia, atrial fibrillation, sinoatrial block, atrioventricular pathway block, left bundle branch block and right bundle branch block, which may affect the judgment of exercise ECG results; 10. Researchers think that there are other factors that are not suitable to participate in the trial; If one of the

Design outcomes

Primary

MeasureTime frameDescription
the difference of HRR between the experimental group and the placebo group was significantAt the end of treatment (8 weeks (± 1 week))Definition of abnormal heart rate recovery: peak HR during exercise - HR one minute into recovery at the end of exercise is defined as abnormal heart rate recovery when HR one minute into recovery is less than 12 beats / min.

Countries

China

Contacts

Primary ContactHaiMing Shi, doctor
13901824859@163.com+8613901824859
Backup ContactYing Shan, doctor
shanyingli@yahoo.com+8613402021699

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026