Swiss Trauma Registry

Trauma Clinical Trial

Official title:

Observational Retrospective and Prospective Registry With Standardized Data Collection on Trauma Treatment in Switzerland

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03526029
• Other study ID #: 2013-00331; ch18Jakob2
• Status: Recruiting
• 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
• 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

Related Conditions & MeSH terms

• Multiple Trauma
• Trauma
• Trauma, Multiple
• Wounds and Injuries

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