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

NCT04086147 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 86

Last updated 2022-03-31

No results posted yet for this study

Summary

To select the best dosage 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

Low dose tenecteplase

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

DRUG

High dose tenecteplase

Intravenous (IV) tenecteplase 0.32 mg/kg (single bolus; maximum dose 32 mg)

Sponsors & Collaborators

  • The First Affiliated Hospital of Shanxi Medical University

    collaborator OTHER
  • Ningbo No. 1 Hospital

    collaborator OTHER
  • Zhejiang Province People's Hospital

    collaborator UNKNOWN
  • Shanghai 5th People's Hospital

    collaborator OTHER
  • Shanghai 10th People's Hospital

    collaborator OTHER
  • Shanghai 6th People's Hospital

    collaborator OTHER
  • The Second Affiliated Hospital of Chongqing Medical University

    collaborator OTHER
  • The Second People's Hospital of Huai'an

    collaborator OTHER
  • Pu'er City People's Hospital

    collaborator UNKNOWN
  • ShuGuang Hospital

    collaborator OTHER
  • Shanghai East Hospital

    collaborator OTHER
  • First People's Hospital of Shenyang

    collaborator OTHER
  • Huashan Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-12-09
Primary Completion
2021-12-31
Completion
2021-12-31

Countries

  • China

Study Locations

More Related Trials

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 NCT04086147 on ClinicalTrials.gov