Status:

UNKNOWN

Personalizing Aspirin Therapy in Peripheral Arterial Disease Patients

Lead Sponsor:

Unity Health Toronto

Collaborating Sponsors:

University of Toronto

Conditions:

Peripheral Arterial Disease

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

Antiplatelet therapies are important to decrease the morbidity and mortality associated with Peripheral Arterial Disease (PAD) through the prevention of thrombus formation. Aspirin (ASA) is a readily ...

Eligibility Criteria

Inclusion

  • Self-reported intake of either 81 mg of aspirin per day for 3 or more days
  • Diagnosed with peripheral arterial disease

Exclusion

  • Alcohol ingestion 24 hours prior to blood draw
  • Patients receiving glycoprotein (GP) IIb/IIIa antagonists
  • Ingestion of a non steroidal anti-inflammatory drug 3 days prior to blood draw
  • History of bleeding disorders
  • Gastrointestinal bleeding
  • Hemorrhagic stroke
  • Allergy to aspirin or ticagrelor
  • Pregnancy, thrombocytopenia anmia or leukopenia

Key Trial Info

Start Date :

November 1 2020

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

November 1 2021

Estimated Enrollment :

150 Patients enrolled

Trial Details

Trial ID

NCT04269863

Start Date

November 1 2020

End Date

November 1 2021

Last Update

October 26 2020

Active Locations (0)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 0 (0 locations)

No Results Found

We couldn’t find results for the location/zipcode entered or within the selected range. Please check your input or adjust your search.

Personalizing Aspirin Therapy in Peripheral Arterial Disease Patients | DecenTrialz