Pretreatment of Acute Coronary Syndrome With Dual Antiplatelet Agents
NCT ID: NCT07039149
Last Updated: 2025-11-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
200 participants
OBSERVATIONAL
2025-08-01
2026-11-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Adult patients admitted for acute coronary syndrome via the ED
Patients with ACS presenting to the ED with a planned coronary angiography for possible coronary revascularization who get aspirin in the ED will be evaluated for bleeding and major cardiovascular events when they receive a second antiplatelet agent in the ED compared with in the cath lab.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Presenting with acute coronary syndrome (ST segment elevation myocardial infarction, non ST segment elevation myocardial infarction, and unstable angina).
* Antiplatelet medication (s) prescribed during index admission to hospital.
* Willingness of the patient to be called for follow up up to 1 year after index hospitalization.
Exclusion Criteria
* No administration of antiplatelet agents during hospitalization.
* Refusal of contact for follow up.
18 Years
ALL
No
Sponsors
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Jordan Collaborating Cardiology Group
OTHER
Responsible Party
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Ayman J Hammoudeh, MD, FACC
Director, Department of Clinical Research; Director, Department of Internal Medicine
Locations
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Jordan University Hospital
Amman, , Jordan
Istishari Hospital
Amman, , Jordan
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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DATES.2.25/irbIH1725
Identifier Type: -
Identifier Source: org_study_id
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