Ignite Creation Date:
2024-05-06 @ 2:34 AM
Last Modification Date:
2024-10-26 @ 11:20 AM
Study NCT ID:
NCT02072538
Status:
WITHDRAWN
Last Update Posted:
2015-05-12
First Post:
2014-02-24
Brief Title:
Pre-discharge vs Early Post-discharge Stress Testing and GRACE Score for Safe Discharge of ACS-patients With a Negative Hs-troponin T Result
Sponsor:
University Hospital Heidelberg
Organization:
University Hospital Heidelberg
Study Overview
Official Title:
Role of Pre-discharge vs Early Post-discharge Stress Testing and Implementation of the GRACE Risk Score for Safe Discharge of Patients With an ACS and a Negative High Sensitivity Troponin T Result Within 3 Hours After Presentation to a Chest Pain Unit
Status:
WITHDRAWN
Status Verified Date:
2015-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
no Sponsor
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
New high-sensitivity cardiac troponin hs-cTn assays allow earlier detection of acute myocardial infarction AMI Furthermore elevated values were associated with an increased risk of recurrent AMI or death Therefore guidelines recommend an early invasive strategy in patients with elevated admission values and kinetic changes Other criteria for an early invasive strategy include a GRACE risk score 140 points or other cardiovascular risk factors Hs-cTn assays allow discrimination of patients at very low and high risk Studies confirmed safety of early discharge protocols in patients with unstable angina UAP The aim of this study is to 1 confirm the safety of early discharge without invasive strategy in patients with UAP and to 2 review the optimal timing of stress-testing Therefore patients are being randomized into 2 groups with pre-discharge and early post-discharge stress-testing Endpoints are major adverse cardiovascular events within 30 and 90 days
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None