Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
Myeloperoxidase and Multi-Markers In the Diagnosis of Diagnoses of Acute Coronary Syndrome (MIDAS) - Sample Procurement
NCT00415948 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of the study is to procure blood samples from patients who present to the Emergency Department with suspected ACS (Acute Coronary Syndrome).
Conditions Studied
Interventions
- DEVICE Biomarkers
Study Locations (18)
Massachusetts
- Beth Israel Deaconess Medical Center — Boston
- Brigham & Women's Hospital — Boston
- Massachusetts General Hospital — Boston
Michigan
- Henry Ford Health System — Detroit
- Spectrum Health Hospitals — Grand Rapids
- Ingham Regional Medical Center — Lansing
Virginia
- University of Virginia — Charlottesville
- Sentara Norfolk General Hopsital — Norfolk
- Virginia Commonwealth University Medical Center — Richmond
New York
- New York Methodist Hosptial — Brooklyn
- SUNY Stony Brook — Stony Brook
North Carolina
- Duke University Medical Center — Durham
- Wake Forest University School of Medicine — Winston-Salem
Ohio
- Cleveland Clinic Foundation — Cleveland
- Ohio State University Medical Center — Columbus
California
- UC Davis — Sacramento
Connecticut
- Yale University — New Haven
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 300 participants |
| Start Date | 2006-12 |
| Est. Completion | 2008-06 |
Interested in This Trial?
Always speak with your doctor before enrolling in a clinical trial.
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00415948
The ClinicalTrials.gov registry entry for NCT00415948 describes a study currently listed as completed. 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 300 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Abbott RDx Cardiometabolic, which has 3 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 Acute Coronary Syndrome (ACS) appearing as the primary indexed condition, and to 1 intervention — of which Biomarkers is the first listed. 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: NCT00415948 reports 18 study locations spanning 9 distinct geographic areas — top geographies include Massachusetts, Michigan, Virginia. 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 NCT00415948 about?
NCT00415948 is a clinical study titled "Myeloperoxidase and Multi-Markers In the Diagnosis of Diagnoses of Acute Coronary Syndrome (MIDAS) - Sample Procurement". The purpose of the study is to procure blood samples from patients who present to the Emergency Department with suspected ACS (Acute Coronary Syndrome).
What is the current status of trial NCT00415948?
This trial is currently completed. The enrollment target is 300 participants. The study started on 2006-12. Estimated completion is 2008-06.
What conditions does trial NCT00415948 study?
This clinical trial studies the following conditions: Acute Coronary Syndrome (ACS). These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00415948?
The interventions under investigation include: Biomarkers (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00415948?
This trial is sponsored by Abbott RDx Cardiometabolic, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00415948 being conducted?
This trial has 18 study locations across California, Connecticut, Maryland, Massachusetts, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
How Clinical Trials Work
Understand phases 1-4, trial design, randomization, and the informed consent process.
Patient Rights in Clinical Trials
Your rights as a participant: consent, withdrawal, privacy, and who to contact.
Finding the Right Clinical Trial
A practical guide to searching trials, understanding eligibility, and evaluating options.
All Guides
Browse our complete library of clinical trial educational resources.
Read our methodology — how this data is sourced, computed, and verified.