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Study on the Registration of Coronary Heart Disease Patients Undergoing PCI

Coronary Heart Disease Clinical Trial

Official title:
Multivariate Analysis of Platelet Reactivity Variety in Patients With Coronary Heart Disease After PCI

Clinical Trial Summary

Study on the registration of coronary heart disease patients undergoing PCI in Chinese's population. Get the incidence of adverse events in these patients after PCI, a clear type of adverse reaction, forms, influencing factors, to establish risk management processes, clinical safety and reasonable treatment, and provide the basis for further research and reference.

Clinical Trial Description

Dual antiplatelet therapy, comprising a low-dose aspirin and a kind of P2Y12 Receptor Inhibitors, has been the mainstay of the management in patients with acute coronary syndromes and/or undergoing Percutaneous Coronary Intervention (PCI). While variability to P2Y12 receptor inhibitors is common in patients and is a major cause of adverse cardiovascular events. Low response to P2Y12 receptor inhibitors will result high platelet reactivity (HPR) and patients who exhibit HPR are at increased risk of atherothrombotic occlusion events. Vice versa, high response to P2Y12 receptor inhibitors will lead to low platelet reactivity (LPR) and increase the risk of hemorrhage.Now, the absence of a universal definition of therapeutic window for different racial and actual clinical situations and lacking the gold standard test to quantify it limit the use in clinic practice.So this clinical trial try to use patient's platelet reactivity combine with type of adverse reaction, forms, influencing factors to find a proper therapeutic windows for P2Y12 receptor inhibitors in Chinese people. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02888652
Study type Observational [Patient Registry]
Source The Third Xiangya Hospital of Central South University
Contact
Status Completed
Phase
Start date September 2015
Completion date October 2018
View Details
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