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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 weeks
Treatment ~ Varies
Follow Up ~1 year
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 year for reporting.

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

Frequently Asked Questions

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~13 spots leftby Apr 2025