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Antiplatelet Agent

Treatment for Heart Attack (CAMEO Trial)

N/A
Recruiting
Led By Tracy Wang, MD
Research Sponsored by Chiesi USA, Inc.
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 the time frame is hospitalization, up to 7 days post discharge
Awards & highlights

Summary

The purpose of this registry is to address optimal platelet inhibition during the early management of MI patients prior to coronary angiography or CABG.

Eligible Conditions
  • Heart Attack

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~the time frame is hospitalization, up to 7 days post discharge
This trial's timeline: 3 weeks for screening, Varies for treatment, and the time frame is hospitalization, up to 7 days post discharge for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Number of bleeding events during hospitalization as measured by medical record report
The number of Antiplatelet medications used during hospitalization

Find a Location

Who is running the clinical trial?

Duke UniversityOTHER
2,424 Previous Clinical Trials
3,062,084 Total Patients Enrolled
Chiesi USA, Inc.Lead Sponsor
8 Previous Clinical Trials
2,104 Total Patients Enrolled
Tracy Wang, MDPrincipal InvestigatorDuke University
2 Previous Clinical Trials
8,877 Total Patients Enrolled
~67 spots leftby Oct 2024