Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
130

Summary

Conditions
Percutaneous Coronary Intervention
Type
Interventional
Phase
Phase 4
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 89 years
Gender
Both males and females

Description

Hypothesis The primary question the investigators propose to answer is whether all patients undergoing PCI with stent deployment who receive chewed ticagrelor will demonstrate more rapid drug absorption and decreased platelet reactivity as compared to integral pill form 1 hour after drug administrat...

Hypothesis The primary question the investigators propose to answer is whether all patients undergoing PCI with stent deployment who receive chewed ticagrelor will demonstrate more rapid drug absorption and decreased platelet reactivity as compared to integral pill form 1 hour after drug administration. Secondary Hypotheses: Major adverse cardiac and cerebrovascular event (MACCE) rate at 30 days and 1 year. Death Repeat myocardial infarction Need for urgent revascularization Cerebrovascular accident Rate of stent thrombosis and in-stent stenosis at 30 days and 1 year. Bleeding: Defined as major, minor, or minimal bleeding based on TIMI criteria.

Tracking Information

NCT #
NCT03708588
Collaborators
Not Provided
Investigators
Principal Investigator: Thomas F Wilson, MD Aurora Health Care