Viewing Study NCT06051110



Ignite Creation Date: 2024-05-06 @ 7:34 PM
Last Modification Date: 2024-10-26 @ 3:09 PM
Study NCT ID: NCT06051110
Status: RECRUITING
Last Update Posted: 2024-02-12
First Post: 2023-09-04

Brief Title: Individual Patient Data Meta-analysis on Prehospital Risk Assessment in Patients Suspected of Non-ST-segment Elevation Acute Coronary Syndrome
Sponsor: Catharina Ziekenhuis Eindhoven
Organization: Catharina Ziekenhuis Eindhoven

Study Overview

Official Title: Individual Patient Data Meta-analysis on Prehospital Risk Assessment in Patients Suspected of Non-ST-segment Elevation Acute Coronary Syndrome
Status: RECRUITING
Status Verified Date: 2024-02
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: None
Brief Summary: Patients with a non-ST-segment elevation acute coronary syndrome NSTE-ACS are currently transported and admitted to the nearest emergency department ED for risk stratification diagnostic workup and treatment Recently several prospective studies have been performed on the diagnostic performance of point-of-care POC-troponin and combined risk scores CRS for pre-hospital risk assessment and triage of NSTE-ACS patients Also the first intervention trials on triage decisions based on POC troponin and CRS have been performed Initial results are indicating that prehospital triage based on these diagnostic tools is feasible and safe although sample sizes were relatively small and underpowered to detect differences in major adverse cardiac events MACE The objective of this individual patient data meta-analysis is to determine the diagnostic performance of POC troponin and combined risk scores for prehospital risk assessment and triage in suspected NSTE-ACS patients
Detailed Description: None

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