Swiss Trauma Registry

Sponsor

University Hospital, Basel, Switzerland (Other)

Overall Status

Recruiting

CT.gov ID

NCT03526029

Collaborator

(none)

2,000

Enrollment

Locations

312

Anticipated Duration (Months)

166.7

Patients Per Site

0.5

Patients Per Site Per Month

Study Details

Study Description

Brief 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.

Condition or Disease	Intervention/Treatment	Phase
Trauma, Multiple Trauma

Study Design

Study Type:

Observational [Patient Registry]

Anticipated Enrollment :

2000 participants

Observational Model:

Cohort

Time Perspective:

Other

Official Title:

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

Actual Study Start Date :

Jan 1, 2015

Anticipated Primary Completion Date :

Dec 31, 2040

Anticipated Study Completion Date :

Dec 31, 2040

Outcome Measures

Primary Outcome Measures

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

Eligibility Criteria

Criteria

Ages Eligible for Study:

16 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

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

Contacts and Locations

Locations

	Site	City	Country	Postal Code
1	Kantonspital Aarau	Aarau	Switzerland	5001
2	University Hospital Switzerland, Traumatology	Basel	Switzerland	4031
3	Inselspital Bern	Bern	Switzerland	3010
4	Kantonsspital Graubünden	Chur	Switzerland	7000
5	University Hospital Geneva	Geneva	Switzerland	1211
6	CHUV	Lausanne	Switzerland	1011
7	Ospedale regionale die Lugano	Lugano	Switzerland	6900
8	Kantonsspital Luzern	Luzern	Switzerland	6000
9	Gesundheitsnetz Wallis	Sion	Switzerland	1951
10	Kantonspital St.Gallen	ST. Gallen	Switzerland	9007
11	Knatonsspital Winterthur	Winterthur	Switzerland	8401
12	University Hospital Zürich	Zürich	Switzerland	8091

Sponsors and Collaborators

University Hospital, Basel, Switzerland

Investigators

Principal Investigator: Marcel Jakob, Prof MD, University Hospital, Basel, Switzerland

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

University Hospital, Basel, Switzerland

ClinicalTrials.gov Identifier:

NCT03526029

Other Study ID Numbers:

2013-00331; ch18Jakob2

First Posted:

May 16, 2018

Last Update Posted:

Jun 3, 2021

Last Verified:

Jun 1, 2021

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Additional relevant MeSH terms:

Wounds and Injuries

Multiple Trauma

Study Results

No Results Posted as of Jun 3, 2021