Pretreatment of Acute Coronary Syndrome With Dual Antiplatelet Agents

NCT ID: NCT07039149

Last Updated: 2025-11-28

Study Results

Results pending

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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Recruitment Status

RECRUITING

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-08-01

Study Completion Date

2026-11-01

Brief Summary

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This is a chart review of data on use of antiplatelet (AP) medications for acute coronary syndrome in the ER. Guidelines recommend giving aspirin in the ER and a second AP agent in the cath lab. What is the outcome when the 2 agents are given n the ER?

Detailed Description

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Dual antiplatelet therapy (DAPT) is a standard treatment in ST-elevation myocardial infarction (STEMI) and non-ST-segment-elevation acute coronary syndrome (NSTEACS) . However, the timing of initiation of DAPT in the Emergency Department (ED) has been defined by recent western guidelines (i.e., aspirin in the ER and and a second AP agent when the coronary anatomy has been denied in the cath lab. This strategy aims at decreasing the incidence of bleeding events. However, patients with ACS in the Middle East are younger than those in the West and have lower bleeding risk. The purpose of this study is to evaluate the incidence of major bleeding in patients who received DAPT in the ED according to the discretion of the treating physician.

Conditions

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Major Bleeding Major Adverse Cardiovascular and Cerebrovascular Events (MACCE)

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

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

* Adult patients
* 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

* Non cardiac chest pain.
* No administration of antiplatelet agents during hospitalization.
* Refusal of contact for follow up.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Jordan Collaborating Cardiology Group

OTHER

Sponsor Role lead

Responsible Party

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Ayman J Hammoudeh, MD, FACC

Director, Department of Clinical Research; Director, Department of Internal Medicine

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Jordan University Hospital

Amman, , Jordan

Site Status RECRUITING

Istishari Hospital

Amman, , Jordan

Site Status NOT_YET_RECRUITING

Countries

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Jordan

Central Contacts

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Ayman Hammoudeh, MD, FACC

Role: CONTACT

+96265001000

Laith Habahbeh, MD

Role: CONTACT

065001000

Facility Contacts

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Ayman Hammoudeh, MD, FACC

Role: primary

065001000

Ayman Hammoudeh, MD, FACC

Role: primary

065001000

Laith Habahbeh, MD

Role: backup

065001000

Other Identifiers

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DATES.2.25/irbIH1725

Identifier Type: -

Identifier Source: org_study_id

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