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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00363753
Other study ID # UCSD IRB #060452
Secondary ID
Status Withdrawn
Phase Phase 1
First received
Last updated
Start date August 2006
Est. completion date March 2007

Study information

Verified date July 2019
Source University of California, San Diego
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Pilot study of continuing aspirin versus switching to clopidogrel after stroke or transient ischemic attack.


Description:

Pilot study of continuing aspirin versus switching to clopidogrel after stroke or transient ischemic attack.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date March 2007
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age 18 and older.

- Stroke or transient ischemic attack (TIA) while taking aspirin within one week of consent.

- Women of child-bearing potential will be included only if there is a negative pregnancy test and they agree to birth control during the treatment period.

Exclusion Criteria:

- Any medical indication for a specific antiplatelet agent (aspirin, clopidogrel, ticlopidine, aggrenox), or an indication for a combination of antiplatelet agents.

- Any medical indication for anticoagulation, except subcutaneous heparin for deep vein thrombosis prophylaxis.

- Allergy to aspirin or clopidogrel.

Study Design


Intervention

Drug:
aspirin versus clopidogrel


Locations

Country Name City State
United States UCSD San Diego California
United States UCSD Hillcrest San Diego California

Sponsors (1)

Lead Sponsor Collaborator
University of California, San Diego

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary mRS at three months.
Secondary Incidence of stroke at three months, bleeding events.
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