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
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
- Cardioembolic Stroke
- Atrial Fibrillation
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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