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Derivation and verification of adverse events prediction after antiplatelet therapy based on pulse wave technology

Evaluation of the efficacy of the big data health management system on the antithrombotic treatment of coronary heart disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100042608
Enrollment
Unknown
Registered
2021-01-24
Start date
2021-01-27
Completion date
Unknown
Last updated
2021-05-03

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

Conditions

Cardiovascular diseases

Interventions

Ischemia :NA
Bleeding :NA

Sponsors

Sixth Medical Center of Chinese People's Liberation Army General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who have been diagnosed with coronary heart disease and are treated with antiplatelet drugs, including patients (PCI, CABG) before and after surgery.

Exclusion criteria

Exclusion criteria: 1. Patients with systemic active infection; 2. Patients with severe liver and kidney insufficiency (ALT>135mmol/L, Cr>200umol/L) or chronic obstructive pulmonary disease; 3. Patients with obvious bleeding tendency and blood diseases Patients; 4. Patients with malignant tumors and end-stage diseases; 5. The life expectancy of patients is less than 6 months; 6. Patients with heart valve disease or left ventricular aneurysm and other diseases requiring simultaneous surgery; 7. Patients with cerebrovascular disease (currently or 6 months Have had cerebral infarction or cerebral hemorrhage within a month); 8. Participated in the trial drug research recently but failed to complete the primary endpoint or clinically hindered the clinical research endpoint; 9. Have been treated with antithrombotic drugs.

Design outcomes

Primary

MeasureTime frame
Adverse event rate;

Countries

China

Contacts

Public ContactYe Weihua

Sixth Medical Center of Chinese People's Liberation Army General Hospital

yeweihua71@sina.com+86 13681389177

Outcome results

None listed

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