The Prognosis of Patients After PCI:a Multi-center Study in China

NCT05614050 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 2400

Last updated 2025-06-26

No results posted yet for this study

Summary

Coronary artery disease (CAD) is caused by myocardial ischemia, hypoxia or necrosis due to coronary artery stenosis, spasm or obstruction. Although standard drug therapy can greatly improve the prognosis of patients with CAD after percutaneous coronary interventions (PCI), these patients are still at high risk of major adverse cardiovascular and cerebrovascular events (MACCE). At present, the concept of residual inflammation risk (RIR) has aroused widespread concern. RIR is an important independent risk in patients with CAD. Previous studies indicated that hsCRP ≥ 2mg / L was the definition standard of RIR in CAD in European and American people. In China, the impact of dynamic changes of hsCRP and other inflammatory factors on MACCE in PCI population remains unclear. Therefore, in this study, the investigators plan to recruit patients undergoing PCI, and observe the impact of hsCRP and other inflammatory factors on the prognosis of these patients during long term follow-up at 17 hospitals in China.

Conditions

Sponsors & Collaborators

  • Shandong Provincial Hospital

    collaborator OTHER_GOV
  • The First Affiliated Hospital of Zhengzhou University

    collaborator OTHER
  • The First Affiliated Hospital of Xiamen University

    collaborator OTHER
  • Shanxi Cardiovascular Hospital

    collaborator OTHER
  • First People's Hospital of Xianyang

    collaborator OTHER
  • Yichang Central People's Hospital

    collaborator OTHER
  • Jingzhou Central Hospital

    collaborator OTHER
  • The First Hospital of Wuhan

    collaborator UNKNOWN
  • Wuhan Central Hospital

    collaborator OTHER
  • Wuhan Fourth Hospital

    collaborator UNKNOWN
  • Fifth Hospital in Wuhan

    collaborator UNKNOWN
  • Chinese Academy of Medical Sciences, Fuwai Hospital

    collaborator OTHER
  • Wuhan Asia Heart Hospital

    collaborator OTHER
  • The First Affiliated Hospital of Anhui Medical University

    collaborator OTHER
  • Central Hospital of Enshi Tujia and Miao Autonomous Prefecture

    collaborator UNKNOWN
  • Hubei University of Medicine

    collaborator OTHER
  • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

    lead OTHER

Principal Investigators

  • Xiang Cheng, Doctor · Department of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-11-01
Primary Completion
2027-11-01
Completion
2027-11-01

Countries

  • China

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05614050 on ClinicalTrials.gov