Ignite Creation Date:
2024-05-06 @ 7:46 PM
Last Modification Date:
2024-10-26 @ 3:13 PM
Study NCT ID:
NCT06128317
Status:
RECRUITING
Last Update Posted:
2023-11-14
First Post:
2023-11-07
Brief Title:
Myocardial Infarction Registry
Sponsor:
University Hospital Heidelberg
Organization:
University Hospital Heidelberg
Study Overview
Official Title:
Cardiac Biochemical and Omics-based Biomarkers in Patients Presenting Symptoms of Acute Coronary Syndrome in the Emergency Department ACS Registry
Status:
RECRUITING
Status Verified Date:
2023-11
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
MIR
Brief Summary:
The single-center MIR-registry was created to assess real-world prevalence demographic characteristics and management of patients with acute coronary syndrome presenting in the emergency department ED of University of Heidelberg
Detailed Description:
To conduct a comprehensive characterization of patients with symptoms of acute coronary syndrome or elevated troponin levels Records include clinical routine parameters there will be an expansion involving the collection of blood samples for the analysis of novel laboratory-based and omics-based biomarkers The ACS registry is monothetically managed by the Department of Internal Medicine III at Heidelberg University Hospital and is intended to serve as a basis for further clinical diagnostic and outcome studies The blood samples will serve as the foundation for a comprehensive analysis of established and novel laboratory-based markers as well as omics-based biomarkers miRNA metabolomics and proteomics Follow-up was performed via review of medical reports phone calls and postal queries The outcome parameters comprised rates for all-cause mortality non-hemorrhagic stroke myocardial infarction and hospitalization for any cause
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None