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Opportunities and Limitations of Swiss Polytrauma Registry Data for Scientific Purposes- Registry Data for Scientific Purposes

Opportunities and Limitations of Swiss Polytrauma Registry Data for Scientific Purposes- Registry Data for Scientific Purposes

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03999346
Enrollment
500
Registered
2019-06-26
Start date
2018-11-01
Completion date
2019-12-12
Last updated
2019-12-18

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

Conditions

Trauma

Keywords

Swiss Polytrauma Registry, quality control, standardized identification procedures, data capture

Brief summary

The aim of the analysis is an evaluation of the current performance of the Swiss Trauma Registry (STR) with respect to providing a reliable basis for (scientific) investigations on the management of trauma patients in Switzerland. The current project tries to address this question by considering central aspects of completeness and by exemplifying the use of the registry for research questions. The aim is to identify potential shortcomings of the registry.

Interventions

OTHERretrospective analysis of the Swiss Trauma Registry data

retrospective analysis of protectively documented registry data based on data completeness, patient outcomes, patient characteristics

Sponsors

University Hospital, Basel, Switzerland
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* documentation in the STR * Injury Severity Score (ISS) ≥ 16

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frameDescription
analysis of data completenesssingle time point assessment at baselineThe STR comprises patient data starting from preclinical management, resuscitation, hospitalization and discharge data as well as data considering 28-day mortality, long-term outcome and cost. The founders agreed on a total of 98 items for analyses. All data sets will be evaluated for completeness of the 98 data points (items).
rate of 28 day survivalsingle time point assessment at baselineanalysis of patient outcome: rate of patients' 28 day survival
length of hospital staysingle time point assessment at baselineanalysis of patient outcome: length of hospital stay (days)
rate of patients receiving intensive care treatmentsingle time point assessment at baselineanalysis of patient outcome: rate of patients receiving intensive care treatment
rate of patients returning to the previous living situationsingle time point assessment at baselineanalysis of patient outcome: rate of patients returning to the previous living situation

Secondary

MeasureTime frameDescription
cost of maintenance of the registersingle time point assessment at baselineanalysis of how many pro-rata salary per cent annually are specifically invested in the maintenance of the register

Countries

Switzerland

Outcome results

None listed

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