Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03526029
Other study ID # 2013-00331; ch18Jakob2
Secondary ID
Status Recruiting
Phase
First received
Last updated
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
Health authority
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

Study Design


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
See also
  Status Clinical Trial Phase
Recruiting NCT04848376 - Post-Market Clinical Follow-up Study of A-SPINE's Products
Terminated NCT03781817 - Intranasal Versus Intravenous Ketamine for Procedural Sedation in Children With Non-operative Fractures Phase 4
Completed NCT04342416 - Using a Brief Visuospatial Interference Intervention to Reduce Intrusive Memories Among Trauma Exposed Women N/A
Recruiting NCT04856449 - DBT Skills Plus EMDR for BPD and Trauma N/A
Completed NCT04356963 - Adjunct VR Pain Management in Acute Brain Injury N/A
Completed NCT05669313 - The Effects of Hypothermia and Acidosis on Coagulation During Treatment With Rivaroxaban Measured With ROTEM
Active, not recruiting NCT03622632 - Pilot Study to Measure Uric Acid in Traumatized Patients: Determinants and Prognostic Association
Recruiting NCT04725721 - Testing FIRST in Youth Outpatient Psychotherapy N/A
Active, not recruiting NCT05530642 - An Augmented Training Program for Preventing Post-Traumatic Stress Injuries Among Diverse Public Safety Personnel N/A
Not yet recruiting NCT05649891 - Checklists Resuscitation Emergency Department N/A
Not yet recruiting NCT03696563 - FreeO2 PreHospital - Automated Oxygen Titration vs Manual Titration According to the BLS-PCS N/A
Withdrawn NCT03249129 - Identification of Autoantibodies and Autoantigens in the Cerebrospinal Fluid of Patients With Spinal Cord Trauma
Completed NCT02240732 - Surgical Tourniquets and Cerebral Emboli N/A
Completed NCT02227979 - Effects of PURPLE Cry Intervention N/A
Withdrawn NCT01169025 - Fentanyl vs. Low-Dose Ketamine for the Relief of Moderate to Severe Pain in Aeromedical Patients N/A
Recruiting NCT01812941 - Evaluation of Mitochondrial Dysfunction in Severe Burn and Trauma Patients N/A
Completed NCT03112304 - Child STEPS for Youth Mental Health in Maine Sustainability N/A
Completed NCT01475344 - Fibrinogen Concentrate (FGTW) in Trauma Patients, Presumed to Bleed (FI in TIC) Phase 1/Phase 2
Completed NCT01201863 - Neuroendocrine Dysfunction in Traumatic Brain Injury: Effects of Testosterone Therapy Phase 4
Completed NCT01210417 - Trauma Heart to Arm Time N/A