EROSION II: OCT Guided PPCI in STEMI

NCT03062826 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 347

Last updated 2022-06-27

No results posted yet for this study

Summary

This protocol describes a prospective, multi-center study intended to test the hypothesis that patients with STEMI caused by plaque rupture or plaque erosion without obstructive stenosis (diameter stenosis \<70%) can be stabilized by effective antithrombotic treatment without stent implantation, thereby avoiding both early and late complications related to percutaneous coronary intervention (PCI) with stent implantation. All the patients will be followed by intracoronary OCT and physiological assessment at 1-month and 12-month follow-up.

Conditions

  • ST-segment Elevation Myocardial Infarction

Interventions

DRUG

dual antiplatelet therapy (aspirin + ticagrelor or aspirin + clopidogrel)

Patients who met the inclusion criteria will be treated with dual antiplatelet therapy (aspirin + ticagrelor or aspirin + clopidogrel).

Sponsors & Collaborators

  • Shenzhen Salubris Pharmaceuticals Co., Ltd.

    collaborator INDUSTRY
  • Beijing Luhe Hospital

    collaborator OTHER
  • The First Hospital of Jilin University

    collaborator OTHER
  • China-Japan Union Hospital, Jilin University

    collaborator OTHER
  • The First Affiliated Hospital of Dalian Medical University

    collaborator OTHER
  • Shanxi Cardiovascular Hospital

    collaborator OTHER
  • Second Hospital of Shanxi Medical University

    collaborator OTHER
  • Hebei General Hospital

    collaborator OTHER
  • General Hospital of Ningxia Medical University

    collaborator OTHER
  • Sichuan Provincial People's Hospital

    collaborator OTHER
  • Affiliated Hospital of Jiangsu University

    collaborator OTHER
  • Xiamen Cardiovascular Hospital, Xiamen University

    collaborator OTHER
  • Shenzhen Sun Yat-sen Cardiovascular Hospital

    collaborator OTHER
  • LanZhou University

    collaborator OTHER
  • Sir Run Run Shaw Hospital

    collaborator OTHER
  • Wuhan Asia Heart Hospital

    collaborator OTHER
  • Harbin Medical University

    lead OTHER

Principal Investigators

  • Bo YU, MD, PhD · The Second Affiliated Hospital of Harbin Medical University

Eligibility

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

Timeline & Regulatory

Start
2017-01-11
Primary Completion
2022-02-24
Completion
2023-03-01

Countries

  • China

Study Locations

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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 NCT03062826 on ClinicalTrials.gov