Prevention of Coronary Slow Flow or No-Reflow During PPCI in Patients With Acute STEMI

NCT03406819 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1000

Last updated 2018-01-23

No results posted yet for this study

Summary

Primary percutaneous coronary intervention (PPCI) is the gold standard of treatment of ST segment elevation myocardial infarction (STEMI).Slow flow / no-reflow phenomenon following PPCI in STEMI patients has been a serious and common complication that closely related to the incidence of major adverse cardiovascular events (MACE) and affected patients' prognosis. No reflow is a multi-factorial phenomenon. And its preventive and therapeutic effects are not satisfactory. This prospective randomized controlled study aimed to compare favorable effects of Nitroprusside versus Tirofiban on the prevention of slow flow / no-reflow phenomenon during PPCI.

Conditions

  • ST Segment Elevation Myocardial Infarction
  • Primary Percutaneous Coronary Intervention

Interventions

DRUG

Nitroprusside Sodium

Intracoronary infusion 50\~100μg each time (repeated)

DRUG

Tirofiban Hydrochloride

Intracoronary infusion 10μg/kg for single time

DRUG

Heparinized saline

Intracoronary infusion 2ml for single time

Sponsors & Collaborators

  • Anyang Regional Hospital

    collaborator OTHER
  • Huaihe Hospital of Henan University

    collaborator OTHER
  • The First Affiliated Hospital of Henan University of Science and Technology

    collaborator OTHER
  • Yellow River Sanmenxia hospital

    collaborator UNKNOWN
  • The Peoples' Hospital of Jiaozuo City

    collaborator OTHER
  • Jincheng People's Hospital

    collaborator OTHER
  • The second people's Hospital of Jiyuan

    collaborator UNKNOWN
  • Kaifeng Central Hospital

    collaborator OTHER
  • Lushan People's Hospital

    collaborator UNKNOWN
  • Nanyang Central Hospital

    collaborator OTHER
  • The Second People's Hospital of Pingdingshan

    collaborator UNKNOWN
  • Shenma Medical Group General Hospital

    collaborator OTHER
  • Puyang People's Hospital

    collaborator UNKNOWN
  • Puyang Oilfield General Hospital

    collaborator OTHER
  • The First People's Hospital of Shangqiu

    collaborator UNKNOWN
  • Yanshi People's Hospital

    collaborator UNKNOWN
  • The First People's Hospital of Xinmi

    collaborator UNKNOWN
  • First Affiliated Hospital of Xinjiang Medical University

    collaborator OTHER
  • Xinyang Central Hospital

    collaborator OTHER
  • People's Hospital of Zhengzhou University

    collaborator OTHER
  • Zhengzhou First People's Hospital

    collaborator UNKNOWN
  • Chinese Academy of Medical Sciences, Fuwai Hospital

    collaborator OTHER
  • Zhengzhou Central Hospital

    collaborator OTHER
  • The 99th Central Hospital of the People's Liberation Army

    collaborator UNKNOWN
  • Zhoukou Central Hospital

    collaborator OTHER
  • The First People's Hospital of Zhumadian

    collaborator UNKNOWN
  • Zhumadian Central Hospital

    collaborator OTHER
  • The First Affiliated Hospital of Zhengzhou University

    lead OTHER

Principal Investigators

  • Chunguang Qiu, Phd · The First Affiliated Hospital of Zhengzhou University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-07
Primary Completion
2018-12-31
Completion
2019-12-31

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 NCT03406819 on ClinicalTrials.gov