Skip to content

EUMIC transport study

Quality and efficacy of interclinical critical transport in the Euregion Meuse-Rhine: An international, prospective, observational, multicentre study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON27738
Enrollment
3000
Registered
2014-12-10
Start date
2015-04-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

interclinical transport, MICU, critical ill transportation, quality measurement,

Interventions

none

Sponsors

Maastricht University Medical Centre+
Lead Sponsor

Eligibility

Inclusion criteria

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

Exclusion criteria: Age < 18 years Interclinical transport without indication for direct supervision of a physician

Design outcomes

Primary

MeasureTime frame
To validate the QUIT EMR score in a prospective multicentre study by comparing three defined levels of transport systems.

Secondary

MeasureTime frame
a)To analyse if negative transport outcome (measured by QUIT EMR score) influences 24-hour post transport morbidity (measured by SEMROS). b)To detect patients’ characteristics that define the patients’ needs in terms of level of transportation facility. c)To detect predictive outcome parameters concerning 24 hours post transport mortality

Contacts

Public ContactU. Strauch

Department of Intensive Care P.O.Box 5800

u.strauch@mumc.nl0031-43-3876385

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)