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Loading dose of Shexiang Tongxin Dripping Pills combined with dual antiplatelet therapy before PCI on myocardial protection in ACS patients

Loading dose of Shexiang Tongxin Dripping Pills combined with dual antiplatelet therapy before PCI on myocardial protection in ACS patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-16009785
Enrollment
Unknown
Registered
2016-11-08
Start date
2017-01-01
Completion date
Unknown
Last updated
2021-12-13

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

Conditions

Coronary Heart Disease

Interventions

Control group:Standard dual antiplatelet therapy only
Intervention group:Loading dose of Shexiang Tongxin Dripping Pills combined with dual antiplatelet therapy

Sponsors

Shanghai Xinhua Hospital affiliated to Shanghai Jiaotong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients (40 to 80 years of age) with unstable angina pectoris (unstable angina was diagnosed when there were new or worsening symptoms of ischemia or changing symptom pattern, and ischemic electrocardiograph changes with normal biomarkers) undergoing elective PCI were randomized to receive STDP plus DAPT or DAPT alone.

Exclusion criteria

Exclusion criteria: 1. Allergies or intolerance to clopidogrel/aspirin; 2. The use of P2Y12 receptor antagonist or immunosuppressive agent within the past six months; 3. A recent history of active bleeding, or infection, or acquired immunodeficiency syndrome; 4. Acute ST-segment elevation myocardial infarction undergoing emergency PCI; 5. Malignant tumors, severe liver or kidney disease, abnormal blood coagulation, or low platelet count (< 100,000/L); 6. A history of major surgery within 6 months; 7. Heart failure (New York Heart Association Classification III or above); 8. Participation in any other trial within the past one month. All patients signed informed consent forms.

Design outcomes

Primary

MeasureTime frame
PMP;

Secondary

MeasureTime frame
Inflammatory cytokines;hsTnI;CKMB;MACEs;

Countries

China

Contacts

Public ContactMeng Shu

Shanghai Xinhua Hospital affiliated to Shanghai Jiaotong University School of Medicine

msdoctor@126.com+86 13916005250

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026