Red Blood Cell Distribution Width and Charlson Comorbidity Indeces in the Frail Polytraumatized Patient.
NCT ID: NCT05221476
Last Updated: 2024-11-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
400 participants
OBSERVATIONAL
2012-01-31
2015-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Danger Response in Polytrauma Patients
NCT02682550
Trauma Associated Bleeding: Effectiveness of an Early Coagulation Support Protocol
NCT03354559
Haemorrhage From Severe Neck and Facial Injuries - Characteristics, Management and Outcomes
NCT07204405
Leukocyte Depletion of Autologous Whole Blood
NCT00176124
Incidence of Trauma Induced Coagulopathy in Patients With Prehospital Administration of Fibrinogen
NCT03572309
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
polytraumatized patients
Patients with an ISS \>16 points, an AIS \>3 in one body region and at least 2 different body regions affected were included.
retrospective
The investigators retrospectively analyzed the short- and long-term outcome in polytraumatized patients and the possible influence of RDW values on admission as well as preexisting comorbidities on these outcomes.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
retrospective
The investigators retrospectively analyzed the short- and long-term outcome in polytraumatized patients and the possible influence of RDW values on admission as well as preexisting comorbidities on these outcomes.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* AIS \>3 in one body region
* at least 2 body regions affected
Exclusion Criteria
* isolated traumatic brain injury
* minor injuries (AIS \<3 or ISS \<16 points)
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Medical University of Vienna
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Dr. Valerie Weihs
MD
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
RDW Polytrauma
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.