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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01757483
Other study ID # D5130L00009
Secondary ID
Status Completed
Phase N/A
First received December 18, 2012
Last updated December 8, 2015
Start date November 2012
Est. completion date December 2014

Study information

Verified date December 2015
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority Canada: Health Canada
Study type Observational

Clinical Trial Summary

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.


Description:

Effectiveness of risk minimisation interventions for ticagrelor in Canada


Recruitment information / eligibility

Status Completed
Enrollment 244
Est. completion date December 2014
Est. primary completion date December 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

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

Exclusion Criteria:

- Participation in a previous wave of the survey.

Study Design

Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
Canada Research Site Montreal Quebec

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary KAU Questionnaire: Knowledge of the 4 key safety issues pertaining to ticagrelor (adequate or inadequate for each safety issue) 2 months Yes
Secondary KAU Questionnaire: Practice characteristics 2 months No
Secondary KAU Questionnaire: The difference in knowledge of understanding across the key safety concerns 2 months No
Secondary KAU Questionnaire: Association between prescribers' characteristics and knowledge and understanding of the key safety concerns. 2 months No
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