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Canadian Ticagrelor Survey

AstraZeneca logo

AstraZeneca

Status

Completed

Conditions

Acute Coronary Syndrome

Study type

Observational

Funder types

Industry

Identifiers

NCT01757483
D5130L00009

Details and patient eligibility

About

This study is designed to evaluate the effectiveness of the current ticagrelor risk minimisation strategy in Canada through a prescriber knowledge and understanding (KAU) survey of selected important identified safety concerns (i.e., bleeding, dyspnea and drug interactions) and ASA dosage.

Full description

Effectiveness of risk minimisation interventions for ticagrelor in Canada

Enrollment

244 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • N/A (All prescribers will be contacted for participation)

Exclusion criteria

  • Participation in a previous wave of the survey.

Trial design

244 participants in 1 patient group

Prescribers

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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