CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 159 enrolled
Drug / intervention
Blood sample collectionother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02713048
NCT02713048N/ACompleted

Sensitive Troponin I and Coronary Anatomy in Patients With Out-of-hospital Cardiac Arrest

University Medical Centre Ljubljana·observational·Posted Mar 18, 2016·Updated Oct 11, 2018

In Brief

An observational study evaluating Blood sample collection for Cardiac Arrest and 3 related conditions. Completed, enrolled 159 participants across 1 site.

Detailed Summary

Troponin is a major diagnostic criterion of acute myocardial infarction (AMI) which confirms myocardial damage and necrosis. In out-of-hospital cardiac arrest (OHCA) patients its dynamics and diagnostic value is often controversial and has not been well described. Most of prior studies were retrospective, using first generation troponin assays and assessing only admission troponin. The aim of this work is to correlate dynamics of sensitive troponin I with urgent coronary angiography. Patients resuscitated after OHCA will be prospectively divided in three groups based on the results of their urgent angiographies. Serial assessment of sensitive troponin I will be obtained over initial 48 hours. We expect admission troponin will not be predictive of AMI. Over next hours troponin levels will be highest in patients with acute coronary lesion, lower in stable obstructive coronary disease and insignificant in non-obstructive coronary disease. We also expect significant difference in highest values and dynamics of troponin in sub-group with spontaneous reperfusion (TIMI flow 2 and 3) comparing to patients with coronary occlusion (TIMI flow 0 and 1). In patients with non-obstructive disease we expect troponin levels to correlate with duration of cardiac arrest, number of external electric shocks and cumulative dose of adrenaline administered.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesSlovenia
Collaborators--

Timeline

N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedMar 18, 2016
Enrollment StartOct 1, 2011
Primary CompletionOct 1, 2018
TodayJul 2, 2026
Enrollment to primary: 7 yearsPosted 10.3 years ago

Interventions

Blood sample collectionother

Eight blood samples in each patient within 48 hours to perform Troponin I measurement.