Stroke Clinical Trial
Official title:
Pilot Study of Continuing Aspirin Versus Switching to Clopidogrel After Stroke or Transient Ischemic Attack
| Verified date | July 2019 |
| Source | University of California, San Diego |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
Pilot study of continuing aspirin versus switching to clopidogrel after stroke or transient ischemic attack.
| Status | Withdrawn |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. |
| Country | Name | City | State |
|---|---|---|---|
| United States | UCSD | San Diego | California |
| United States | UCSD Hillcrest | San Diego | California |
| Lead Sponsor | Collaborator |
|---|---|
| University of California, San Diego |
United States,
| 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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