Implementation of prehospital high Sensitive troponin and risk Stratification- validation phase
Phase 3
Withdrawn
- Conditions
- Acute coronary syndroomchest pain10019280
- Registration Number
- NL-OMON53821
- Lead Sponsor
- Ambulancezorg Rotterdam-Rijnmond ARR
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Withdrawn
- Sex
- Not specified
- Target Recruitment
- 300
Inclusion Criteria
In order to be eligible to participate in this study, a subject must meet all
of the following criteria: >= 18 age with acute chest pain suggestive of cardiac
chest pain or acute coronary syndrome.
Exclusion Criteria
A potential subject who meets any of the following criteria will be excluded
from participation in this study: ST-elevation on ECG, new left bundle branch
block, systolic blood pressure below 90 mmHg, tachycardia above 140 beats per
minute, clinical instability, signs of acute heart failure, terminal kidney
failure, pregnancy, life expectancy of less than 3 months, obvious non cardiac
cause of acute chest pain, inability to provide a written informed consent or
inappropriate knowledge of English or Dutch language.
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Agreement of Troponin measurement between central laboratory and POCT device,<br /><br>numerical and as part of the HEART score. </p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary objective is the ease of use, time spent performing the test.</p><br>