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The Multifunctional Image Guided Therapy Suite (MIGTS) in Emergency Multiple Trauma Care

The Impact of a Multifunctional Image Guided Therapy Suite (MIGTS) on Emergency Multiple Trauma Care - a Controlled Clinical Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00772213
Acronym
MIGTS
Enrollment
168
Registered
2008-10-15
Start date
2003-02-28
Completion date
2005-04-30
Last updated
2013-10-30

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

Conditions

Acceleration of Procedure, Involved Staff Member's Evaluation, Reduction of Number of Transports and Transfers

Keywords

multiple trauma, outcome and process assessment

Brief summary

Controlled clinical intervention study comparing the treatment of multiple trauma patients in a newly developed combined diagnostic and operation room, the multifunctional image guided therapy suite (MIGTS) versus controls. The MIGTS proved to significantly accelerate the procedure and led to more satisfied team members.

Detailed description

Objective: Pilot evaluation to which extend the implementation of a newly developed combined diagnostic and operation room, the multifunctional image guided therapy suite (MIGTS) may influence the emergency treatment of multiply injured patients. Summary Background: Controlled data on the impact of modern technology integration in multiple trauma management and involved care providers are lacking. Methods: Quasi-randomized clinical intervention study comparing the treatment of multiple trauma patients (injury severity score, ISS \>16) in the MIGTS versus controls.

Interventions

PROCEDUREMIGTS treatment

treatment of multiple trauma patients in the MIGTS

Sponsors

Swiss National Science Foundation
CollaboratorOTHER
Scientific Foundation of the Swiss Accident Insurance Fond
CollaboratorUNKNOWN
Voluntary Academic Society, Basel
CollaboratorUNKNOWN
CARCAS Switzerland
CollaboratorUNKNOWN
University Hospital, Basel, Switzerland
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* multiple trauma with * at least two abbreviated injury scoring (AIS) regions involved and * injury severity score (ISS)\>16 * primary hospital treatment at University Hospital Basel

Exclusion criteria

* monotrauma or * ISS \< 16 or * prior treatment in another hospital

Design outcomes

Primary

MeasureTime frame
Time to first CT scanfirst CT scan after arrival of emergency patient

Secondary

MeasureTime frame
Staff member evaluation (Likert scale 1-5)end of emergency treatment (arrival ICU or death)

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026