Early Administration of Heparin At FMC for PPCI of STEMI Patients

NCT05329155 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1145

Last updated 2025-03-27

No results posted yet for this study

Summary

Heparin is the first choice of anticoagulation drug for primary PCI of STEMI patients. However, the priority of use of hepairn in first medical contact or in Cathlab has not yet studied. Previous study revealed early use of antithrombotic drugs could improve patient's survival. Here we supposed that use of heparin at first medical contact could increase the TIMI flow 3 grade ratio in STEMI patients and improve patient's survival and/or reduce MACE rather than in Cathlab.

Conditions

  • STEMI
  • Primary PCI

Interventions

DRUG

Heparin Sodium Injection

Heparin Sodium Injection (100U/Kg body weight)

Sponsors & Collaborators

  • Xiangyang Central Hospital

    collaborator OTHER
  • The Central Hospital of Enshi Tujia And Miao Autonomous Prefecture

    collaborator OTHER
  • Wuhan Central Hospital

    collaborator OTHER
  • People's Hospital of Jingshan

    collaborator UNKNOWN
  • Chibi General Hospital

    collaborator UNKNOWN
  • Xianning Central Hospital

    collaborator OTHER
  • Hubei University of Medicine

    collaborator OTHER
  • Yichang Central People's Hospital

    collaborator OTHER
  • People's Hospital of Tongcheng

    collaborator UNKNOWN
  • Ezhou Central Hospital

    collaborator UNKNOWN
  • Xiantao First People's Hospital

    collaborator UNKNOWN
  • Songzi People's Hospital

    collaborator UNKNOWN
  • Anlu People's Hospital

    collaborator UNKNOWN
  • Caidian People's Hospital

    collaborator UNKNOWN
  • Jiangxia First People's Hospital

    collaborator UNKNOWN
  • Jingzhou Central Hospital

    collaborator OTHER
  • Hubei Zhongshan Hospital

    collaborator UNKNOWN
  • Guoyao Dongfeng General Hospital

    collaborator UNKNOWN
  • Wuhan Puren Hospital

    collaborator OTHER
  • Shiyan People's Hospital

    collaborator UNKNOWN
  • General Hospital of Yangtze River shipping

    collaborator UNKNOWN
  • Fifth Hospital in Wuhan

    collaborator UNKNOWN
  • CR & WISCO General Hospital

    collaborator UNKNOWN
  • Xishui People's Hospital

    collaborator UNKNOWN
  • Jiangling People's Hospital

    collaborator UNKNOWN
  • Wuhan Third Hospital

    collaborator OTHER
  • Laohekou First Hospital

    collaborator UNKNOWN
  • The Central Hospital of Huanggang

    collaborator OTHER
  • Wuhan No.1 Hospital

    collaborator OTHER
  • Hanyang University

    collaborator OTHER
  • Wuxue First People's Hospital

    collaborator UNKNOWN
  • Tianmen First People's Hospital

    collaborator UNKNOWN
  • Xianning First People's Hospital

    collaborator UNKNOWN
  • Wuhan No.6 Hospital

    collaborator UNKNOWN
  • Wuhan Hospital of Traditional Chinese Medicine

    collaborator OTHER
  • Renmin Hospital of Wuhan University

    lead OTHER

Principal Investigators

  • Jing Chen, PhD · Renmin Hospital of Wuhan University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2022-07-20
Primary Completion
2023-08-20
Completion
2024-08-20

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 NCT05329155 on ClinicalTrials.gov