TraumaNCT07492758
Management of Extremity Injuries Registry
An observational study of Trauma, run by Methodist Health System at 1 site in United States.
Trial summary
The primary objective of this study is to establish a data set that will be permissive of quality improvement studies/observations specific to life and limb salvage in comprisable extremity injuries. Read more about this study
- Who is it for?
- Ages 16 years and older
- Conditions the study is for
- Trauma
- What is being tested?
- Non-Interventional (Registry)
- How many people
- 999 participants
- Where
- 1 siteUnited States
- Study dates
- 31 Oct 2023to 12 Jun 2025
- How long will I take part?
- 5 Years
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 16 years and older
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: Adult trauma patients; defined by the American College of Surgeons as individuals age: ≥16 years, identified in the MDMC trauma registry with documented extremity injury.
Who may be able to join
- Adult trauma patients; defined by the American College of Surgeons as individuals age: ≥16 years
- Included in the MDMC trauma registry
- Documented extremity injury
Who cannot join
- <16 years old
Trial locations and contacts
1 site in 1 country.
United States1 site
Clinical Research Institute at Methodist Health System
Dallas, Texas, 75203
About this study
The primary objective of this study is to establish a data set that will be permissive of quality improvement studies/observations specific to life and limb salvage in comprisable extremity injuries.
Read the detailed description
Tourniquets are often overused. Direct pressure should be the first step in STB. Combat dressings allow for hands free pressure. These data could provide a foundation for pre-hospital process improvement studies.
This data repository will serve as a means to aggregate and analyze best practices related to trauma patients with extremity injuries. Specific interest will be placed in best practices of the emergency medical service and trauma bay, use of tourniquets and compression bandages, ischemic injuries, and limb salvage.
- Conditions
- Trauma
- Being tested
- Non-Interventional (Registry)
- Medical subject headings
- Wounds and Injuries
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Non-Interventional (Registry)Other
Non-Interventional (Registry)
What is being measured
The primary outcome is the main question the study is designed to answer.
establish a data set that will be permissive of quality improvement studies/observations specific to life and limb salvage in comprisable extremity injuries.
Trauma Registry will be queried for demographic information, admission dates, traumatic injury characteristics, inpatient outcomes, complications, consultations, resuscitation strategies, compression time to control bleeding, use of tourniquet and indications, discharge location, and mortality. Additional triage assessments, bleeding management, and in-patient timeline, will be abstracted from EPIC.
Measured: through study completion, up to 18 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Mar 2026
- Study start31 Oct 2023
- Primary completion12 Jun 2025
- Study completion12 Jun 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for TraumaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Cross-sectional
- Enrolment
- 999 participants (actual)
- Target duration
- 5 Years
Sponsor and investigators
- Lead sponsor
- Methodist Health System
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Conner McDaniel, MD, Principal investigator, Methodist Heath System
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07492758
- Sponsor's protocol ID
- 039.TRA.2023.D
- Status last verified
- Oct 2024
- First submitted
- 14 Nov 2024
- Last updated
- 25 Mar 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 25 Mar 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Management of Extremity Injuries Registry
- ClinicalTrials.gov ID
- NCT07492758
- Acronym / sponsor ID
- 039.TRA.2023.D
- Conditions
- Trauma
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 999 participants (actual)
- Lead sponsor
- Methodist Health SystemUniversity, hospital or other
- Study start
- 31 Oct 2023 (actual)
- Primary completion
- 12 Jun 2025 (actual)
- Study completion
- 12 Jun 2025 (actual)
- First posted
- 25 Mar 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The primary objective of this study is to establish a data set that will be permissive of quality improvement studies/observations specific to life and limb salvage in comprisable extremity injuries.
Detailed description
Tourniquets are often overused. Direct pressure should be the first step in STB. Combat dressings allow for hands free pressure. These data could provide a foundation for pre-hospital process improvement studies.
This data repository will serve as a means to aggregate and analyze best practices related to trauma patients with extremity injuries. Specific interest will be placed in best practices of the emergency medical service and trauma bay, use of tourniquets and compression bandages, ischemic injuries, and limb salvage.
Study design
- Observational model
- Other
- Time perspective
- Cross-sectional
- Target follow-up
- 5 Years
Who may qualify
- Ages
- 16 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Adult trauma patients; defined by the American College of Surgeons as individuals age: ≥16 years, identified in the MDMC trauma registry with documented extremity injury.
Key inclusion criteria (3 listed)
- Adult trauma patients; defined by the American College of Surgeons as individuals age: ≥16 years
- Included in the MDMC trauma registry
- Documented extremity injury
Key exclusion criteria (1 listed)
- <16 years old
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Non-Interventional (Registry)Non-Interventional (Registry) | Other | – |
Primary outcome
establish a data set that will be permissive of quality improvement studies/observations specific to life and limb salvage in comprisable extremity injuries.
Time frame: through study completion, up to 18 months
Trauma Registry will be queried for demographic information, admission dates, traumatic injury characteristics, inpatient outcomes, complications, consultations, resuscitation strategies, compression time to control bleeding, use of tourniquet and indications, discharge location, and mortality. Additional triage assessments, bleeding management, and in-patient timeline, will be abstracted from EPIC.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 25 Mar 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Conner McDaniel, MD principal investigator
Methodist Heath System
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Trauma, run by Methodist Health System at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 25 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
establish a data set that will be permissive of quality improvement studies/observations specific to life and limb salvage in comprisable extremity injuries. (time frame: through study completion, up to 18 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Mar 2026.