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Clinical Trial 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.


Clinical Trial Description

The CAMEO registry is a multicenter observational registry that will collect information on 4,000 patients with NSTEMI or STEMI treated with cangrelor or an oral P2Y12 inhibitor into the registry. Phase 1: Each site will abstract data from the medical record for the first 50 patients meeting the inclusion and exclusion criteria treated at the hospital within 4 months prior to study initiation or during the study period. Phase 2: After Phase 1, all cangrelor-treated patients meeting the inclusion and exclusion criteria treated at the hospital no later than 1 month from the discharge date will be entered into the registry, and we will begin sampling non-cangrelor patients in a 2:1 cangrelor: non-cangrelor ratio. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04076813
Study type Observational
Source Chiesi USA, Inc.
Contact Leo Brothers
Phone 919-668-8322
Email joseph.l.brothers@duke.edu
Status Recruiting
Phase
Start date October 16, 2019
Completion date October 31, 2024

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