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Clinical study for treatment of angina pectoris after coronary intervention with Kuanxiong Aerosol

Clinical study for treatment of angina pectoris after coronary intervention with Kuanxiong Aerosol

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027006
Enrollment
Unknown
Registered
2019-10-28
Start date
2019-05-17
Completion date
Unknown
Last updated
2020-04-20

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

Conditions

angina pectoris after coronary intervention

Interventions

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for angina pectoris after coronary intervention (both meet the following two): (1) Within 1 year after coronary intervention; (2) angina; 2. angina pectoris 2 times a week or more; 3. Patients aged 18 to 85 years; 4. Chinese medicines for treating angina pectoris are not used, or are discontinued for 2 weeks or more; and the variety and dosage of anti-angina pectoris medicines are not incereased within 2 weeks (including: beta Receptor blockers, non-dihydropyridine calcium ion antagonists;except nitroglycerin tablets; 5. The patient is willing to follow up and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Those who are allergic to the Kuanxiong Aerosol or the ingredients contained (asarone oil, sandalwood oil, galangal oil, eucalyptus oil, borneol); 2. Can't or don't want to sign an informed consent form; 3. Continued severe angina (CCS Level IV); 4. In the past, severe ST-segment depression occurred during exercise test level 1; 5. In the past, cardiac ultrasound examination revealed a left ventricular ejection fraction (LVEF) 2 times the upper limit of normal reference); 10. Any other serious disease or condition such as a malignant tumor; 11. Uncontrolled severe hypertension (systolic blood pressure > 180 mmHg, diastolic blood pressure > 110 mmHg) 12. Severe arrhythmia (such as rapid atrial fibrillation, ventricular tachycardia, high atrioventricular block, etc.) 13. Have participated in another clinical study within 30 days before the screening period or have received randomization of the study; 14. Pregnant women or women preparing to become pregnant; 15. The investigator judged that the patient was not eligible to participate in the study.

Design outcomes

Primary

MeasureTime frame
Seattle Angina Questionnaire (SAQ);

Secondary

MeasureTime frame
SF-12 quality of life scale;visual analogue scale of chest pain;Symptom grading quantization table;

Countries

China

Contacts

Public ContactQiuxiong Chen

Guangdong Provincial Hospital of Chinese Medicine

eric1961chen@aliyun.com+86 13902230066

Outcome results

None listed

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