Actively Recruiting

Age: 15Years - 100Years
All Genders
ID07208110

Factors Associated With Mortality by Trauma in the Intensive Care Unit in Villavicencio, Colombia. A Trial Based on a Discharge Registry.

Led by Hospital Departamental de Villavicencio · Updated on 2026-05-27

500

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

H

Hospital Departamental de Villavicencio

Lead Sponsor

C

Cooperative University of Colombia

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are investigating the factors linked to severe trauma outcomes, including mortality, among patients admitted to intensive care units (ICUs) in general hospitals across the Colombian Orinoco region. This study focuses on trauma, the leading cause of death and disability in young populations worldwide, often caused by violence and vehicle accidents. By analyzing trauma admissions and comparing them to other ICU admissions, the study aims to identify key predictors of trauma mortality and outcomes. The study involves reviewing ICU discharge records over a two-year period from January 2022 to December 2024 at two hospitals in Villavicencio, Colombia. Patients are grouped into those admitted for trauma-related reasons and those admitted for other diagnoses. The researchers will analyze demographic data, severity scores, and diagnoses to understand differences and factors associated with trauma outcomes. Participants' medical records will be examined to assess mortality within 30 days and length of ICU stay. The study will highlight causes of trauma admissions, severity, and outcomes for different trauma types. The goal is to develop a predictive model tailored to the local population to help improve resource allocation, treatment strategies, and potentially reduce mortality and complications. The study extends through 2028 and is observational, reviewing existing hospital data without direct patient intervention.

CONDITIONS

Brief Title

Mortality of Trauma in the Intensive Care Unit.

Who Can Participate

Age: 15Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Admitted to the intensive care unit
  • Aged between 15 and 100 years
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surveillance

Duration - Up to 30 days

Participants who undergo routine intensive care unit admission are observed and their records reviewed to analyze factors associated with trauma mortality and ICU length of stay.

Observation of hospital stay with no additional visits required

Trial Site Locations

Total: 1 location

1

Hospital Departamental de Villavicencio

Villavicencio, Meta Department, Colombia, 50001

Actively Recruiting

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Research Team

N

Norton Perez Gutierrez, MD

E

Emma I Rodriguez Darabos, MSc

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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