Construction and validation of a nomogram prediction model for the need for intensive care unit admission after hip fracture surgery.
Fang Wang, Zi-Mou Li, Tao Ma
https://pubmed.ncbi.nlm.nih.gov/40527820Actively Recruiting
Led by Hospital Departamental de Villavicencio · Updated on 2026-05-27
500
Participants Needed
1
Research Sites
N/A
Total Duration
H
Hospital Departamental de Villavicencio
Lead Sponsor
C
Cooperative University of Colombia
Collaborating Sponsor
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
Mortality of Trauma in the Intensive Care Unit.
You may qualify if you...
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
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
Total: 1 location
1
Hospital Departamental de Villavicencio
Villavicencio, Meta Department, Colombia, 50001
Actively Recruiting
N
Norton Perez Gutierrez, MD
E
Emma I Rodriguez Darabos, MSc
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
Have more questions? Get in touch with our team for quick support
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here
Fang Wang, Zi-Mou Li, Tao Ma
https://pubmed.ncbi.nlm.nih.gov/40527820Cristina Rey Valcarcel, Dan Bieler, Gary A Bass...
https://pubmed.ncbi.nlm.nih.gov/40214785Mariana Sofia Nunes Dos Santos, Louise Caroline Stayt
https://pubmed.ncbi.nlm.nih.gov/40339389Yongzhuang Chen, Xianjie Wei, Xiaoyun Sun...
https://pubmed.ncbi.nlm.nih.gov/40506077A F Hefny, K Idris, H O Eid...
https://pubmed.ncbi.nlm.nih.gov/24250314Minoru Fukuchi, Masanobu Nakajima, Yasuyuki Fukai...
https://pubmed.ncbi.nlm.nih.gov/14712482