Trauma, MultipleNCT03526029
Swiss Trauma Registry
An observational study of Trauma, Multiple and Trauma, run by University Hospital, Basel, Switzerland at 12 sites in Switzerland.
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. Read more about this study
- Who is it for?
- Ages 16 years and older
- Conditions the study is for
- Trauma, Multiple, Trauma
- How many people
- 2,000 participants
- Where
- 12 sitesSwitzerland
- Study dates
- 1 Jan 2015to 31 Dec 2040
- How long will I take part?
- 5 Years
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 16 years and older
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: severely injured patients at hospitals
Who may be able to join
- injury severity code > 16 and 7 or abbreviated injury scale >3 for region of skull and brain
Who cannot join
- patients who will transferred in a burn unit
- drowned patients
Trial locations and contacts
12 sites in 1 country. Contact the study team or a site near you to ask about taking part.
Nicolas Bless, Prof MD contact
Dario Picardi contact
12 sites in 1 country
Switzerland12 sites, 12 recruiting
- Recruiting
Kantonspital Aarau
Aarau, 5001
Thomas Gross, MD, thomas.gross@ksa.ch
- Recruiting
University Hospital Switzerland, Traumatology
Basel, 4031
Nicolas Bless, MD, +41 61 32 ext. 86248, nicolas.bless@usb.ch
- Recruiting
Inselspital Bern
Bern, 3010
Beat Schnueriger, PD MD, beat.schnueriger@insel.ch
- Recruiting
Kantonsspital Graubünden
Chur, 7000
Thomas Müller, MD, thomas.mueller@ksgr.ch
- Recruiting
University Hospital Geneva
Geneva, 1211
Axel Gamulin, MD, axel.gamulin@hsuge.ch
- Recruiting
CHUV
Lausanne, 1011
Catherine Heim, MD, catherine.heim@chuv.ch
- Recruiting
Kantonsspital Luzern
Lucerne, 6000
Jan Rosenkreuz, MD, jan.rosenkreuz@luks.ch
- Recruiting
Ospedale regionale die Lugano
Lugano, 6900
Christian Candrian, MD, christian.candrian@eoc.ch
- Recruiting
Kantonspital St.Gallen
Sankt Gallen, 9007
Joseph Osterwalder, Prof MD, joseph.osterwalder@kssg.ch
- Recruiting
Gesundheitsnetz Wallis
Sion, 1951
Claude Haller, MD, claude.haller@hospitalvs.ch
- Recruiting
Knatonsspital Winterthur
Winterthur, 8401
Severin Meili, MD, severin.meili@ksw.ch
- Recruiting
University Hospital Zürich
Zurich, 8091
Kai Sprengel, MD, kai.sprengel@usz.ch
About this study
Official title: Observational Retrospective and Prospective Registry With Standardized Data Collection on Trauma Treatment in Switzerland
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.
- Conditions
- Trauma, Multiple, Trauma
- Medical subject headings
- Multiple Trauma, Wounds and Injuries
What is being measured
The primary outcome is the main question the study is designed to answer.
mortality in severely injured patients
number of severely injured patients who died
Measured: day of injury until year 5
patterns of injuries in severely injured patients
comparison of patterns of injuries in severely injured patients
Measured: day of injury until year 5
Duration of primary hospitalisation after initial injury measured by days
Duration of primary hospitalisation after initial injury measured by days
Measured: day of injury until year 5
Duration of secondary hospitalisation after initial injury measured by days
Duration of secondary hospitalisation after initial injury measured by days
Measured: day of injury until year 5
Treatment costs in Swiss Francs
Treatment costs in Swiss Francs
Measured: 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 (kind of treatment)
Measured: day of injury until year 5
line of treatments due to the initial injury (timepoints of treatments)
line of treatments due to the initial injury (timepoints of treatments)
Measured: day of injury until year 5
Duration of Rehabilitation measured by days
Duration of Rehabilitation measured by days
Measured: day of injury until year 5
Duration of incapacity for work measured by days
Duration of incapacity for work measured by days
Measured: day of injury until year 5
diagnostic efforts measured by number and timepoint of imaging
number and timepoint of imaging
Measured: day of injury until year 5
treatment efforts measured by number of medication given
number and timepoint of medication given and medical interventions performed
Measured: day of injury until year 5
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
Measured: on day of primary hospitalisation
treatment efforts measured by number of medical interventions performed
Treatment efforts measured by number and timepoint of medication given and medical interventions performed
Measured: day of injury until year 5
treatment efforts measured by timepoint of medication given
Treatment efforts measured by number and timepoint of medication given and medical interventions performed
Measured: day of injury until year 5
treatment efforts measured by timepoint of medical interventions performed
Treatment efforts measured by number and timepoint of medication given and medical interventions performed
Measured: day of injury until year 5
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 May 2018
- Study start1 Jan 2015
- Primary completion31 Dec 2040 (estimated)
- Study completion31 Dec 2040 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Trauma, MultipleStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Other
- Enrolment
- 2,000 participants (estimated)
- Target duration
- 5 Years
Sponsor and investigators
- Lead sponsor
- University Hospital, Basel, Switzerland
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Andreas Marc Müller, Prof MD, Principal investigator, University Hospital, Basel, Switzerland
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03526029
- Sponsor's protocol ID
- 2013-00331; ch18Jakob2
- Status last verified
- Feb 2025
- First submitted
- 19 Mar 2018
- Last updated
- 19 Feb 2025
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 19 Feb 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Observational Retrospective and Prospective Registry With Standardized Data Collection on Trauma Treatment in Switzerland
- ClinicalTrials.gov ID
- NCT03526029
- Acronym / sponsor ID
- 2013-00331; ch18Jakob2
- Conditions
- Trauma, Multiple, Trauma
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 2,000 participants (estimated)
- Lead sponsor
- University Hospital, Basel, SwitzerlandUniversity, hospital or other
- Study start
- 1 Jan 2015 (actual)
- Primary completion
- 31 Dec 2040 (estimated)
- Study completion
- 31 Dec 2040 (estimated)
- First posted
- 16 May 2018 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Other
- Target follow-up
- 5 Years
Who may qualify
- Ages
- 16 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- severely injured patients at hospitals
Key inclusion criteria (1 listed)
- injury severity code > 16 and 7 or abbreviated injury scale >3 for region of skull and brain
Key exclusion criteria (2 listed)
- patients who will transferred in a burn unit
- drowned patients
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
mortality in severely injured patients
Time frame: day of injury until year 5
number of severely injured patients who died
patterns of injuries in severely injured patients
Time frame: 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
Time frame: 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
Time frame: day of injury until year 5
Duration of secondary hospitalisation after initial injury measured by days
Treatment costs in Swiss Francs
Time frame: day of injury until year 5
Treatment costs in Swiss Francs
line of treatments due to the initial injury (kind of treatment)
Time frame: 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)
Time frame: day of injury until year 5
line of treatments due to the initial injury (timepoints of treatments)
Duration of Rehabilitation measured by days
Time frame: day of injury until year 5
Duration of Rehabilitation measured by days
Duration of incapacity for work measured by days
Time frame: day of injury until year 5
Duration of incapacity for work measured by days
diagnostic efforts measured by number and timepoint of imaging
Time frame: day of injury until year 5
number and timepoint of imaging
treatment efforts measured by number of medication given
Time frame: day of injury until year 5
number and timepoint of medication given and medical interventions performed
Primary supply Dates measured in minutes
Time frame: 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
Time frame: 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
Time frame: 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
Time frame: day of injury until year 5
Treatment efforts measured by number and timepoint of medication given and medical interventions performed
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 Feb 2025.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Nicolas Bless, Prof MD contact
Dario Picardi contact
Andreas Marc Müller, Prof MD principal investigator
University Hospital, Basel, Switzerland
12 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Trauma, Multiple and Trauma, run by University Hospital, Basel, Switzerland at 12 sites in Switzerland.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 19 Feb 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 12 sites in Switzerland. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Nicolas Bless, Prof MD (nicolas.bless@usb.ch), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
mortality in severely injured patients (time frame: day of injury until year 5). The study lists 15 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Feb 2025.