Whole Blood in Trauma Patients With Hemorrhagic Shock
NCT05634109
Accidental Injuries, Hemorrhage
Cali, Valle del Cauca Department, Colombia
View Trial DetailsNCT Number: NCT03526029
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.
Interested in participating?
Request Info16 year and older
All sexes
Observational
Kantonspital Aarau, Aarau, Switzerland
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: day of injury until year 5
number of severely injured patients who died
Time frame: day of injury until year 5
comparison of patterns of injuries in severely injured patients
Time frame: day of injury until year 5
Duration of primary 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
Time frame: day of injury until year 5
Treatment costs in Swiss Francs
Time frame: day of injury until year 5
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 (timepoints of treatments)
Time frame: day of injury until year 5
Duration of Rehabilitation measured by days
Time frame: day of injury until year 5
Duration of incapacity for work measured by days
Time frame: day of injury until year 5
number and timepoint of imaging
Time frame: day of injury until year 5
number and timepoint of medication given and medical interventions performed
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
Time frame: day of injury until year 5
Treatment efforts measured by number and timepoint of medication given and 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
Time frame: day of injury until year 5
Treatment efforts measured by number and timepoint of medication given and medical interventions performed
Contact information is provided by the study sponsor or research team.
University Hospital, Basel, Switzerland
Other
Observational Retrospective and Prospective Registry With Standardized Data Collection on Trauma Treatment in Switzerland
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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