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Clinical Study on Atherosclerotic Cardiovascular Disease with Integrated Traditional Chinese and Western Medicine

Evaluation of the clinical effect of Huoxin Pill on angina pectoris after PCI

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100051805
Enrollment
Unknown
Registered
2021-10-04
Start date
2019-04-16
Completion date
Unknown
Last updated
2021-11-02

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

Conditions

arteriosclerotic cardiovascular disease

Interventions

Case series:Huoxin pill

Sponsors

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 30-75 years old; 2. Patients with angina pectoris symptoms within 12 months after PCI; 3. TCM syndrome differentiation is the syndrome of qi stagnation and blood stasis; 4. The patient signs an informed consent form, has good compliance, and cooperates with follow-up visits and re-examinations.

Exclusion criteria

Exclusion criteria: 1. Diagnosed as STEMI, or diagnosed as NSTEMI who is at high risk by Grace score; 2. Patients with congenital heart disease, severe pulmonary hypertension, malignant tumors, severe COPD; 3. Valvular disease (LVEF1.5 times the upper limit of normal value, Cr>1.2 times the upper limit of normal value (refer to the laboratory test of the research center for normal values Scope); Other clinically significant laboratory tests are abnormal and the investigator determines that it is not suitable to be included in the group; 5. People with allergies or allergic to the experimental drug Huoxin Pills, excipients or similar ingredients; 6. Suspected or true history of alcohol or drug abuse; 7. Pregnant or breastfeeding women or those who have planned pregnancy in the near future and are unwilling to use contraceptive measures; 8. Patients who have participated in other clinical trials within 1 month before enrollment; 9. The investigator believes that it is not suitable for patients to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
Nitroglycerin reduction rate;

Countries

China

Contacts

Public ContactFan Min

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of TCM

13564528699@qq.com+86 13818835654

Outcome results

None listed

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