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ACTIVE NOT RECRUITING

Cangrelor in Acute Myocardial Infarction: Effectiveness and Outcomes Registry

NCT04076813 · View on ClinicalTrials.gov ↗

Study 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.

Conditions Studied

Study Locations (11)

California

  • The Regents of the University of California on behalf of its San Diego campus — La Jolla

Delaware

  • Christiana Care Health Services, Inc. — Newark

Florida

  • University of Florida — Gainesville

Idaho

  • Kootenai Hospital District dba Kootenai Health — Coeur d'Alene

Maryland

  • MedStar Health Research Institute, Inc. — Hyattsville

Massachusetts

  • The Brigham and Women's Hospital, Inc. — Boston

Michigan

  • Henry Ford Health System — Detroit

Missouri

  • Washington University — St Louis

Trial Details

FieldValue
Enrollment Target 5,050 participants
Start Date 2019-10-16
Est. Completion 2025-06-30

Sponsor

Chiesi USA

1 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04076813

The ClinicalTrials.gov registry entry for NCT04076813 describes a study currently listed as active not recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 5,050 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Chiesi USA, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Myocardial Infarction appearing as the primary indexed condition, and to 0 interventions. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT04076813 reports 11 study locations spanning 11 distinct geographic areas — top geographies include California, Delaware, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT04076813 about?

NCT04076813 is a clinical study titled "Cangrelor in Acute Myocardial Infarction: Effectiveness and Outcomes Registry". The purpose of this registry is to address optimal platelet inhibition during the early management of MI patients prior to coronary angiography or CABG.

What is the current status of trial NCT04076813?

This trial is currently active not recruiting. The enrollment target is 5,050 participants. The study started on 2019-10-16. Estimated completion is 2025-06-30.

What conditions does trial NCT04076813 study?

This clinical trial studies the following conditions: Myocardial Infarction. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

Who is sponsoring clinical trial NCT04076813?

This trial is sponsored by Chiesi USA, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04076813 being conducted?

This trial has 11 study locations across California, Delaware, Florida, Idaho, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial