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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05549986
Other study ID # 21MMHIS389e
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2016
Est. completion date December 31, 2020

Study information

Verified date September 2022
Source Mackay Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

We evaluated a cohort of adult trauma patients transported to emergency departments. The first vital signs were used to calculate the SI, MSI, and rSIG. The areas under the receiver operating characteristic curves (AUROCs) and test results were used to compare the discriminant performance of the indices on short-term mortality and poor functional outcome. A subgroup analysis of geriatric patients, traumatic brain injury, penetrating injury, and non-penetrating injury was performed.


Recruitment information / eligibility

Status Completed
Enrollment 105641
Est. completion date December 31, 2020
Est. primary completion date December 31, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adult patients (=18 years) EMS-transported from January 2016 to December 2020 Exclusion Criteria: - Patients with missing entries of age, sex, triage, SBP, DBP, HR, or GCS were excluded. - Entries with missing records of in-hospital mortality or 30-day mortality were excluded from the short-term mortality cohort analyses. - Patients without a Modified Rankin Scale (MRS) record at discharge were excluded from the functional outcome cohort analyses.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Observational
Observational

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Mackay Memorial Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Discriminant power of SI, MSI, and rSIG on short-term mortality for adult traumatic patients AUROC in associated with short-term mortality with SI, MSI, rSIG 30 days
Secondary Discriminant power of SI, MSI, and rSIG on functional outcome for adult traumatic patients AUROC in associated with functional outcome with SI, MSI, rSIG We defined no symptoms, no significant disability, slight disability, and moderate disability (MRS 0-3) as favorable functional outcomes and moderately severe disability, severe disability, and death (MRS 4-6) as poor functional outcomes
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