Trial of pRehospital Intervention With trAditional Chinese Medicine for Acute strokE

NCT04275349 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2020-06-11

No results posted yet for this study

Summary

The main purpose of this trial is to observe whether Xingnaojing, intravenously administered within 24 hours of symptom onset on pre-hospital emergency ambulance, improves the Early neurological deterioration of acute stroke at 3 days.

Conditions

  • Stroke
  • Acute Ischemic Stroke
  • Acute Intracranial Hemorrhage

Interventions

DRUG

Xingnaojing injection within 24 hours of symptom onset

intravenously administered Xingnaojing injection within 24 hours of symptom onset on ambulance or at hospital

Sponsors & Collaborators

  • Beijing Emergency Medical Center

    collaborator OTHER
  • Beijing Tiantan Hospital

    collaborator OTHER
  • Beijing Hospital of Traditional Chinese Medicine

    collaborator OTHER
  • Centre for Evidence Based Chinese Medicine, Beijing University of Chinese Medicine

    collaborator UNKNOWN
  • Xuanwu Hospital, Beijing

    collaborator OTHER
  • Beijing Friendship Hospital

    collaborator OTHER
  • Beijing Chao Yang Hospital

    collaborator OTHER
  • Beijing Shijitan Hospital, Capital Medical University

    collaborator OTHER
  • Beijing Fengtai Youanmen Hospital

    collaborator UNKNOWN
  • Beijing Jiangong Hospital

    collaborator UNKNOWN
  • Beijing Chaoyang Emergency Medical Center

    collaborator UNKNOWN
  • Beijing Chaoyang Integrative Medicine Emergency Medical Center

    collaborator UNKNOWN
  • Guang'anmen Hospital of China Academy of Chinese Medical Sciences

    collaborator OTHER
  • Fangshan Hospital,Beijing University of Chinese Medicine

    collaborator UNKNOWN
  • Civil Aviation General Hospital

    collaborator OTHER
  • The First Hospital of Fangshan District,Beijing

    collaborator OTHER
  • Beijing Chinese Medicine Hospital-Pinggu Hospital

    collaborator UNKNOWN
  • Beijing Pinggu District Hospital

    collaborator OTHER
  • Dongzhimen Hospital, Beijing

    lead OTHER

Principal Investigators

  • Ying Gao, MD · Dongzhimen Hospital, Beijing

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-03-20
Primary Completion
2020-12-31
Completion
2020-12-31

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 NCT04275349 on ClinicalTrials.gov