ClinicalTrials.gg
CompletedNCT07185529Updated Sep 22, 2025

Predictors of Mortality in Multiple Trauma Patients

An observational study in Multiple Trauma/Injuries, sponsored by Melike Cengiz. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-09-22.

Sponsored by Melike Cengiz · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
269
Ages
18 Years and older
Sex
All
01

Study summary

Trauma is a public health concern that causes serious financial and medical burdens worldwide. According to the World Health Organization, 4.4 million people die from traumatic injuries each year which account for about 8% of global deaths. Traumatic injuries are among the most common causes of mortality particularly in young individuals. It also has a negative economic impact due to the loss of labor. Determining the factors associated with mortality in the ICU follow-up and treatment of these patients is very important for clarifying these uncertainties and improving ICU outcomes. The main objective of the study was to ascertain the ICU processes of multipletrauma patients and the factors that may have an effect on mortality.

Read the detailed description

All patients with traumatic injuries severe enough to warrant ICU admission formed the subjects of the study. The study included patients aged 18 years and over who were diagnosed with multiple trauma injuries and admitted to the ICU.The analysis included patients with a final outcome (survival or death) at our centre. Only patients who were admitted to the ICU for the first time were included. The following systems were used to assess the clinical and multiple trauma injury severity at the time of admission to the ICU: the Acute Physiology and Chronic Health Assessment II (APACHE II) score, the Simplified Acute Physiology Score II (SAPS II), the Sequential Organ Failure Assessment (SOFA) score, the Glasgow Coma Scale (GCS), the Injury Severity Score (ISS), the Revised Trauma Score (RTS) and the Trauma and Injury Severity Score (TRISS). All injury severity scores were calculated using clinical findings, imaging results and surgical findings. A comprehensive data set was collated at the time of admission to the intensive care unit, encompassing patient age, gender, comorbidities, and the Charlson Comorbidity Index (CCI). The injury mechanism, blood sugar, haemoglobin and lactate levels, Horowitz index, hypotension and hypothermia were also recorded.The patients were categorised into two groups: survival and mortality

02

Conditions studied

  • Multiple Trauma/Injuries

Keywords

  • Intensive Care Unit
  • Mortality
  • Multiple trauma patient
03

In context

Multiple Trauma

139 studies on the registry are indexed under Multiple Trauma; 32 are open to participants now.

This study's enrollment of 269 is above the median of 200 across 84 observational studies indexed under Multiple Trauma.

Browse Multiple Trauma studies →

Lead sponsor

Melike Cengiz is the lead sponsor of 7 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

The sample included patients with multiple trauma injuries who were admitted in the ICU between 01 January 2021 and 01 November 2023.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients aged ≥18 years with patients with multiple trauma injuries
  • Patients with a final outcome (survival or mortality) in our centre

Exclusion criteria

Exclusion Criteria:

  • Patients with trauma to a single region (head, thorax, abdomen or extremities)
  • Patients who were pregnant
  • Length of intensive care unit stay ≤24 hours
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
269 participants (actual)
Patient registry
No

Groups and cohorts

  • survival

    consists of surviving patients

    Other: Data of the patients were obtained from patient observation files and hospital information system database.

  • mortality

    consists of deceased patients

    Other: Data of the patients were obtained from patient observation files and hospital information system database.

Interventions

  • OtherData of the patients were obtained from patient observation files and hospital information system database.

    Data of the patients were obtained from patient observation files and hospital information system database.

06

What researchers measure

Primary outcomes

  1. The primary outcome of the study is mortality

    Time frame: 01 January 2021 and 01 November 2023

07

Study locations

1 site
  • Akdeniz University
    Antalya, Turkey (Türkiye)
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 22, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07185529
Lead sponsor
Melike Cengiz
Responsible party
Melike Cengiz (professor doctor, Akdeniz University) — Sponsor-investigator
First posted
Sep 22, 2025
Start date
Jan 1, 2021
Primary completion
Nov 1, 2023
Completion
Jul 15, 2025
Last update
Sep 22, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion