Hirudin Plus Aspirin in the Secondary Prevention of Cardioembolic Stroke Due to Nonvalvular Atrial Fibrillation

NCT02181361 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 239

Last updated 2020-04-21

No results posted yet for this study

Summary

To investigate the efficacy and safety of hirudin plus aspirin therapy compared with warfarin in the secondary prevention of cardioembolic stroke due to nonvalvular atrial fibrillation.

Conditions

Interventions

DRUG

hirudin plus aspirin

natural hirudin 0.75g, three times a day (Brand name: Maixuekang capsule, Guizhou Xinbang Pharmaceutical Co., China) and aspirin 100mg, once daily

DRUG

Warfarin

an initial dose of 1.25mg once daily. Three days later, INR of patients was checked every three days and the dose of warfarin was adjusted until reach the target range of 2 to 3. Since then INR monitoring was performed at 1, 2, 3, 6, 9, 12 months after stroke onset, targeting an INR between 2 and 3 and the dose of warfarin was adjusted accordingly.

Sponsors & Collaborators

  • Xi'an Central Hospital

    collaborator OTHER
  • Shaanxi people's Hospital

    collaborator UNKNOWN
  • The Third Hospital of PLA

    collaborator UNKNOWN
  • Hanzhong Central Hospital

    collaborator OTHER
  • Xianyang 215 hospital

    collaborator UNKNOWN
  • Yulin Second Hospital

    collaborator UNKNOWN
  • Yan'an University Affiliated Hospital

    collaborator OTHER
  • Baoji Central Hospital

    collaborator OTHER
  • Ankang Central Hospital

    collaborator OTHER
  • Baoji People's Hospital

    collaborator UNKNOWN
  • Yan'an people's Hospital

    collaborator UNKNOWN
  • 451 Hospital

    collaborator UNKNOWN
  • Shangluo Central Hospital

    collaborator OTHER
  • Central Hospital of China Railway 20th Bureau

    collaborator UNKNOWN
  • Xiangyang Central Hospital

    collaborator OTHER
  • Xi'an Ninth Hospital

    collaborator UNKNOWN
  • Shangluo Second People's Hospital

    collaborator UNKNOWN
  • Xijing Hospital

    lead OTHER

Principal Investigators

  • wen jiang, MD,PhD · The Department of Neurology , Xijing Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-06-30
Primary Completion
2016-12-31
Completion
2018-10-31

Countries

  • China

Study Locations

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Entities

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 NCT02181361 on ClinicalTrials.gov