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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03526029
Other study ID # 2013-00331; ch18Jakob2
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2015
Est. completion date December 31, 2040

Study information

Verified date January 2024
Source University Hospital, Basel, Switzerland
Contact Marcel Jakob, Prof MD
Phone +41 61 556
Email marcel.jakob@usb.ch
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The Swiss Conference of Cantonal Health Directors has transferred the planning of highly specialized medicine to a specialized body under the direction of the Swiss Academy of Sciences. This specialist body has defined the treatment of critically ill as part of highly specialized medicine and founded the Swiss Trauma Registry at 12 hospitals in Switzerland. The registry is designed to provide a consistent and standardized approach and treatment outcomes in the short and long term quality control and as a basis for planning highly specialized medicine.


Recruitment information / eligibility

Status Recruiting
Enrollment 2000
Est. completion date December 31, 2040
Est. primary completion date December 31, 2040
Accepts healthy volunteers No
Gender All
Age group 16 Years and older
Eligibility Inclusion Criteria: - injury severity code > 16 and 7 or abbreviated injury scale >3 for region of skull and brain Exclusion Criteria: - patients who will transferred in a burn unit - drowned patients

Study Design


Locations

Country Name City State
Switzerland Kantonspital Aarau Aarau
Switzerland University Hospital Switzerland, Traumatology Basel
Switzerland Inselspital Bern Bern
Switzerland Kantonsspital Graubünden Chur
Switzerland University Hospital Geneva Geneva
Switzerland CHUV Lausanne
Switzerland Ospedale regionale die Lugano Lugano
Switzerland Kantonsspital Luzern Luzern
Switzerland Gesundheitsnetz Wallis Sion
Switzerland Kantonspital St.Gallen ST. Gallen
Switzerland Knatonsspital Winterthur Winterthur
Switzerland University Hospital Zürich Zürich

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Basel, Switzerland

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary mortality in severely injured patients number of severely injured patients who died day of injury until year 5
Primary patterns of injuries in severely injured patients comparison of patterns of injuries in severely injured patients day of injury until year 5
Primary Duration of primary hospitalisation after initial injury measured by days Duration of primary hospitalisation after initial injury measured by days day of injury until year 5
Primary Duration of secondary hospitalisation after initial injury measured by days Duration of secondary hospitalisation after initial injury measured by days day of injury until year 5
Primary Treatment costs in Swiss Francs Treatment costs in Swiss Francs day of injury until year 5
Primary line of treatments due to the initial injury (kind of treatment) line of treatments due to the initial injury (kind of treatment) day of injury until year 5
Primary line of treatments due to the initial injury (timepoints of treatments) line of treatments due to the initial injury (timepoints of treatments) day of injury until year 5
Primary Duration of Rehabilitation measured by days Duration of Rehabilitation measured by days day of injury until year 5
Primary Duration of incapacity for work measured by days Duration of incapacity for work measured by days day of injury until year 5
Primary diagnostic efforts measured by number and timepoint of imaging number and timepoint of imaging day of injury until year 5
Primary treatment efforts measured by number of medication given number and timepoint of medication given and medical interventions performed day of injury until year 5
Primary Primary supply Dates measured in minutes Primary supply Dates measured by time to start of surgery, time to admission to trauma room, time to ICU admission on day of primary hospitalisation
Primary treatment efforts measured by number of medical interventions performed Treatment efforts measured by number and timepoint of medication given and medical interventions performed day of injury until year 5
Primary treatment efforts measured by timepoint of medication given Treatment efforts measured by number and timepoint of medication given and medical interventions performed day of injury until year 5
Primary treatment efforts measured by timepoint of medical interventions performed Treatment efforts measured by number and timepoint of medication given and medical interventions performed day of injury until year 5
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