CHinese Acute Tissue-Based Imaging Selection for Lysis In Stroke -Tenecteplase II

NCT04516993 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 224

Last updated 2023-11-29

No results posted yet for this study

Summary

To explore the efficacy and safety of tenecteplase for acute ischemic stroke patients (onset time 4.5-24h) of large vessel occlusion using early combined CT/MR imaging outcomes

Conditions

Interventions

DRUG

Tenecteplase

Intravenous (IV) tenecteplase 0.25 mg/kg (single bolus; maximum dose 25 mg)

DRUG

The best treatment selected by local doctors(Aspirin, Recombinant Tissue Plasminogen Activator, Urokinase, Thrombectomy)

Best treatment arm

Sponsors & Collaborators

  • Puer People's Hospital

    collaborator UNKNOWN
  • Shanghai 6th People's Hospital

    collaborator OTHER
  • Hexigten Traditional Chinese and Mongolian Medicine Hospital

    collaborator UNKNOWN
  • Yangpu Hospital, School of Medicine, Tongji University

    collaborator UNKNOWN
  • The First Affiliated Hospital of Shanxi Medical University

    collaborator OTHER
  • Seventh People's Hospital of Shanghai University of Traditional Chinese Medicine

    collaborator UNKNOWN
  • Linyi People's Hospital

    collaborator OTHER
  • Shanghai 10th People's Hospital

    collaborator OTHER
  • Nanshi Hospital of Nanyang

    collaborator UNKNOWN
  • Fudan University

    collaborator OTHER
  • Xuzhou Medical University Affiliated Hospital of Huaian

    collaborator UNKNOWN
  • Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine

    collaborator UNKNOWN
  • The First Affiliated Hospital of Soochow Medical University

    collaborator UNKNOWN
  • Affiliated Haian People's Hospital of Nantong University

    collaborator UNKNOWN
  • First Affiliated Hospital of Harbin Medical University

    collaborator OTHER
  • the Third Hospital of Mianyang

    collaborator UNKNOWN
  • Zhejiang Province People's Hospital

    collaborator UNKNOWN
  • Shanghai East Hospital

    collaborator OTHER
  • The Central Hospital of Jiaozuo Coal Group

    collaborator UNKNOWN
  • Huizhou Municipal Central Hospital

    collaborator OTHER
  • Zhejiang University

    collaborator OTHER
  • The Second Affiliated Hospital of Chongqing Medical University

    collaborator OTHER
  • Ningbo No. 1 Hospital

    collaborator OTHER
  • Huashan Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2021-09-28
Primary Completion
2023-09-30
Completion
2023-09-30

Countries

  • China

Study Locations

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Entities

Diseases

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 NCT04516993 on ClinicalTrials.gov