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Antiplatelet Agent
tailored antiplatelet selection for Stroke (PASSPoRT Trial)
Phase 2
Waitlist Available
Led By Karen C Albright, PhD, DO
Research Sponsored by State University of New York - Upstate Medical University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year
Awards & highlights
PASSPoRT Trial Summary
This study is evaluating whether a precision medicine approach to antiplatelet selection for secondary stroke prevention is safe and feasible.
Eligible Conditions
- Stroke
- Ischemic Stroke
- Mini Stroke
PASSPoRT Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Feasibility - Recruitment and Platelet Reactivity
Safety - Bleeding Complications
Secondary outcome measures
Patient-centered Outcomes - Satisfaction
PASSPoRT Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Treatment GroupExperimental Treatment1 Intervention
Intervention group
Group II: Control GroupActive Control1 Intervention
Standard of Care group
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
tailored antiplatelet selection
2018
Completed Phase 2
~90
Find a Location
Who is running the clinical trial?
State University of New York - Upstate Medical UniversityLead Sponsor
172 Previous Clinical Trials
27,242 Total Patients Enrolled
2 Trials studying Stroke
234 Patients Enrolled for Stroke
Karen C Albright, PhD, DOPrincipal InvestigatorState University of New York - Upstate Medical University
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