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Prospective, open, single-arm, post-marketing clinical trial on the safety and efficacy of Fufang Maqitong Capsule in the treatment of stable coronary heart disease with angina pectoris and cardiac blood stasis syndrome (including patients with mild to moderate hypertension)

Prospective, open, single-arm, post-marketing clinical trial on the safety and efficacy of Fufang Maqitong Capsule in the treatment of stable coronary heart disease with angina pectoris and cardiac blood stasis syndrome (including patients with mild to moderate hypertension)

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068203
Enrollment
Unknown
Registered
2023-02-10
Start date
2023-02-10
Completion date
Unknown
Last updated
2024-06-03

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

Conditions

Stable coronary heart disease (syndrome of cardiac blood stasis)

Interventions

Therapeutic group:Take orally 4 capsules three times a day after meals. 30 days is a course of treatment

Sponsors

Zhejiang Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years old, regardless of gender; 2. Consistent with Western diagnostic criteria for angina pectoris of stable coronary heart disease (refer to 2018 Guidelines for Diagnosis and Treatment of Stable Coronary Heart Disease); 3. The patient has the main symptoms of chest pain and chest tightness, which meets the TCM diagnosis criteria of coronary heart disease, angina pectoris, blood blood stasis syndrome (Appendix 18.3); 4. Sign informed consent voluntarily.

Exclusion criteria

Exclusion criteria: 1. Patients with poor blood pressure control (systolic blood pressure >= 180 mmHg and/or diastolic blood pressure >= 110 mmHg); 2. Patients with severe cardiac insufficiency (cardiac function grade IV), severe arrhythmia and other serious heart diseases; 3. Pregnant and lactating women; 4. Patients with gastric and duodenal ulcers and other gastrointestinal bleeding tendency in the active stage; 5. APTT Upper limit of 1.5 times normal; 6. Abnormal liver and kidney function (ALT, AST, TBIL or SCr greater than 1.5 times the upper limit of normal); 7. Patients who are considered unsuitable for this clinical trial by investigators.

Design outcomes

Primary

MeasureTime frame
physical examination;Vital signs;blood biochemistry;Blood RT;Urinalysis;stool for routine;coagulation function;12-lead electrocardiogram;adverse event;

Secondary

MeasureTime frame
The incidence rate of TCM syndrome efficacy is judged to be obvious and effective;the incidence of angina symptoms were significant or improved;Incidence of discontinuation and halving of medication use for acute angina attacks;

Countries

China

Contacts

Public ContactJing Yan

Zhejiang Hospital

zjicu@vip.163.com+86 571 8159 5216

Outcome results

None listed

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