NCT07490145 · Methodist Health System
Trauma Activation Criteria
What this study is about
To quantify the over- and under-triage rates as relative to trauma activation criteria reform.
View original scientific description
To quantify the over- and under-triage rates as relative to trauma activation criteria reform.
Interventions
OTHER
over- and under-triage rates
To quantify the over- and under-triage rates as relative to trauma activation criteria reform.
Primary outcome measures
Determine the over/under-triage rates
Time frame: 2 year
The project will be evaluated by comparing the over- and under-triage rates of the historical criteria and the reformed criteria. As the criteria reform was live November 25, 2024, pre-implementation will be defined as November 24, 2023 - November 24, 2024 and post-implementation will be defined as November 25, 2024 - November 25, 2025.
Who can participate
This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.
Inclusion criteria
- Patient is included in the Methodist Dallas Medical Center trauma registry. Trauma patients who recieved care at Methodist Dallas Medical Center between November 24, 2023 and November 25, 2025.
Exclusion criteria
- Patient does not meet registry inclusion criteria.
Where
- Dallas, Texas
Related conditions & keywords
Frequently asked questions
What is a clinical trial?
A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.
Is it safe to participate?
Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.
Will I be compensated?
Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.
Will I receive a placebo instead of treatment?
When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.
Can I leave a trial if I change my mind?
Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.
How long does a clinical trial last?
Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.
Data: ClinicalTrials.gov · synced Mar 24, 2026 · Source of record for eligibility and locations