Actively Recruiting

Age: 16Years +
All Genders
ID03526029

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

Age: 16Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surveillance

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

Actively Recruiting

3

Inselspital Bern

Bern, Switzerland, 3010

Actively Recruiting

4

Kantonsspital Graubünden

Chur, Switzerland, 7000

Actively Recruiting

5

University Hospital Geneva

Geneva, Switzerland, 1211

Actively Recruiting

6

CHUV

Lausanne, Switzerland, 1011

Actively Recruiting

7

Kantonsspital Luzern

Lucerne, Switzerland, 6000

Actively Recruiting

8

Ospedale regionale die Lugano

Lugano, Switzerland, 6900

Actively Recruiting

9

Kantonspital St.Gallen

Sankt Gallen, Switzerland, 9007

Actively Recruiting

10

Gesundheitsnetz Wallis

Sion, Switzerland, 1951

Actively Recruiting

11

Knatonsspital Winterthur

Winterthur, Switzerland, 8401

Actively Recruiting

12

University Hospital Zürich

Zurich, Switzerland, 8091

Actively Recruiting

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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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