Recruiting NCT07490171

Traumatic Cardiac Arrest

— Observational Trauma

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied: The protocol lists: Medical/Phenotype Data Collection Procedures & Data to be Collected.
Who it may be relevant to: Registry conditions: Trauma. Basic parameters: from 18 years · All.
What needs checking: Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place: United States
Next step: Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Traumatic Cardiac Arrest Registry

Overview

This retrospective data repository will serve as a means to aggregate and analyze order of pre-hospital care (intubation, medication, etc) as it relates to Traumatic cardiac arrest.

Detailed description

The primary objective of this study is to establish a data repository that will be permissive of quality improvement studies/observations specific to patients with Traumatic cardiac arrest and evaluate impact of sequence of pre-hospital care in survival outcomes.

Interventions

Other Medical/Phenotype Data Collection Procedures & Data to be Collected
The MDMC Trauma Registry will be queried for demographic information, diagnosis codes, admission dates, traumatic injury characteristics, surgical procedures, comorbidities, inpatient outcomes, complications, consultations, discharge location, and mortality. Additional laboratory values will be abstracted from Epic through retrospective chart review.

Primary outcome measures

Total Number of Study Sites [Time frame: 5 years]

Eligibility criteria

Inclusion criteria

≥18 years old Included in the MDMC Trauma Registry Cardiac arrest in pre-hospital setting or trauma bay

Exclusion criteria

<18 years old Prisoners, pregnant persons, or other protected population

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model: Other

Study locations

United States · 1 center

Methodist Dallas Medical Center- Clinical Research Institute — Dallas

Identifiers

NCT: NCT07490171 · 052.TRA.2023.D

Primary sources (government registries)

ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗