Research Site
Montreal, Quebec, Canada
NCT Number: NCT01757483
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.
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Notify Me18 year–85 year
All sexes
Observational
Montreal, Quebec, Canada
Effectiveness of risk minimisation interventions for ticagrelor in Canada
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 2 months
Time frame: 2 months
Time frame: 2 months
Time frame: 2 months
AstraZeneca
Industry
Effectiveness of Risk Minimisation Interventions for Ticagrelor in Canada
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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