EUMIC transport study
- Conditions
- interclinical transport, MICU, critical ill transportation, quality measurement,
- Registration Number
- NL-OMON27738
- Lead Sponsor
- Maastricht University Medical Centre+
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 3000
Inclusion Criteria
Adult patients (18 years) which undergo an interclinical transport with indication for a physician supervised transport within the study region (MICU region Maastricht, district of Aachen, City of Aachen, district of Heinsberg and Düren).
Exclusion Criteria
Age < 18 years
Interclinical transport without indication for direct supervision of a physician
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To validate the QUIT EMR score in a prospective multicentre study by comparing three defined levels of transport systems.
- Secondary Outcome Measures
Name Time Method a)To analyse if negative transport outcome (measured by QUIT EMR score) influences 24-hour post transport morbidity (measured by SEMROS).<br> b)To detect patients’ characteristics that define the patients’ needs in terms of level of transportation facility.<br>c)To detect predictive outcome parameters concerning 24 hours post transport mortality<br>