Mayo Clinic
Rochester, Minnesota, 55905, United States
NCT Number: NCT00276432
The primary outcome in this study will be time to discharge for low-risk patients and therapeutic turnaround time for patients with NSTEMI or unstable angina.
Looking for future studies?
Notify Me21 year and older
All sexes
Interventional
Phase 4
Rochester, Minnesota, 55905, United States
Phase IV prospective, randomized (1:1), parallel-group trial utilizing concurrent controls. Assess the reduction in time taken to dispostion or discharge patients. Assess the ability of POC testing to satisfy guidelines for a 30 minute turn around time of results. Assess and differences in clinical decision-making for other diagnostic procedures including nuclear imaging, echo, and stress treadmill, disposition from the ED, time to catherterization lab, PCI, and CafBG based on the cardiac troponinn results from the bedside analyzer and the central lab instrument.Assess the difference for in-hospital and 30 day post hospital discharge cardiac events including all-cause and cardiac-specific deaths, CHF, cardiomyopathy, and atrial and ventricular arrhythmia, beween the bedside analyzer and the central lab instrument. Assess the differences in hospital care costs for the hospitalization period, and assess direct medical and indirect productivity costs in the 30 day post hospital discharge period to patients who are diagnosed, using the bedside cTnl test and the central lab cTn tests, and subsequently treated as per the guidelines.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Patient must be 21 years old or older with chest pain or other symptoms that lead to drawing cardiac biomarkers.
Mayo Clinic
Other
Diagnosis and Treatment of Acute Coronary Syndrome in the Emergency Department- The Impact of Rapid Bedside cTnl on Outcome.
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT02317198
Angina Pectoris, Angina, Unstable
Nieuwegein, Utrecht, Netherlands
View Trial DetailsNCT00449826
Acute Coronary Syndrome, Angina Pectoris
Ottawa, Ontario, Canada
View Trial DetailsNCT06860997
Acute Coronary Syndrome, Angina Pectoris
Brussels, Belgium
View Trial DetailsNCT06404515
ASCVD, Acute Coronary Syndrome
New York, United States
View Trial Details