Actively Recruiting
Observational Retrospective and Prospective Registry Collecting Standardized Data on Trauma Treatment in Switzerland
Led by University Hospital, Basel, Switzerland · Updated on 2025-02-19
2000
Participants Needed
12
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
The Swiss Trauma Registry is designed to improve the treatment and outcomes of critically injured patients across 12 hospitals in Switzerland. This observational study collects standardized data to monitor and analyze care quality and long-term results for patients with severe trauma. The registry supports planning and quality control of highly specialized trauma medicine under the direction of the Swiss Academy of Sciences. Participants include patients with severe injuries, defined by injury severity codes greater than 16 and specific brain injury assessments. The registry collects data retrospectively and prospectively from the day of injury up to five years. It tracks various treatment and recovery aspects including hospital stays, rehabilitation, medical interventions, medication use, imaging, and costs. Patients' involvement is observational, with no active treatment assigned by the study. Researchers gather detailed information on treatments, timelines, diagnostic efforts, and outcomes such as mortality and work incapacity duration. Data collection spans from the initial hospital stay through long-term follow-up to assess care patterns and resource use. No direct interventions are administered as part of this registry study.
CONDITIONS
Brief Title
Swiss Trauma Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Injury severity code greater than 16 and 7 or abbreviated injury scale greater than 3 for skull and brain region
- Age 16 years or older
You will not qualify if you...
- Patients transferred to a burn unit
- Patients who have drowned
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 5 years from the day of injury
Participants who undergo routine trauma care are observed over time to collect standardized data on injury patterns, treatments, hospitalizations, and recovery.
Data collected during hospital stays and follow-up assessments as per routine care
Trial Site Locations
Total: 12 locations
1
Kantonspital Aarau
Aarau, Switzerland, 5001
Actively Recruiting
2
University Hospital Switzerland, Traumatology
Basel, Switzerland, 4031
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3
Inselspital Bern
Bern, Switzerland, 3010
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4
Kantonsspital Graubünden
Chur, Switzerland, 7000
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5
University Hospital Geneva
Geneva, Switzerland, 1211
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6
CHUV
Lausanne, Switzerland, 1011
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7
Kantonsspital Luzern
Lucerne, Switzerland, 6000
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8
Ospedale regionale die Lugano
Lugano, Switzerland, 6900
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9
Kantonspital St.Gallen
Sankt Gallen, Switzerland, 9007
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10
Gesundheitsnetz Wallis
Sion, Switzerland, 1951
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11
Knatonsspital Winterthur
Winterthur, Switzerland, 8401
Actively Recruiting
12
University Hospital Zürich
Zurich, Switzerland, 8091
Actively Recruiting
Research Team
N
Nicolas Bless, Prof MD
D
Dario Picardi
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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