Ultrasound Assessment of Nutritional Status and Frailty in Surgical ICU Patients
This observational study aims to assess the nutritional status and frailty in surgical ICU patients by measuring adipose tissue thickness, body mass index, clinical frailty scale, length of mechanical ventilation, nutritional risk screening 2002, and the thickness and echogenicity of various muscles using ultrasound.
Data Collection
Collected from today forward - ProspectiveFrailty
+ Pathologic Processes
+ Pathological Conditions, Signs and Symptoms
Other
Utilizing specific methods not covered by standard models in order to address unique research questions.Summary
Study start date: February 1, 2026
Actual date on which the first participant was enrolled.This study focuses on surgical patients in the intensive care unit (ICU). It's common for these patients to be admitted due to older age, multiple health conditions, sepsis, high-risk surgery, or complications during procedures. The study aims to understand how the nutritional status and physical frailty of these patients can predict their recovery time and overall treatment outcome. Nutritional status is typically assessed using measures like body mass index (BMI), blood hemoglobin and albumin levels, and rating scales such as NRS and MUST. Frailty, a condition marked by reduced ability to handle physical and mental changes, is often linked with aging and can predict treatment duration and outcome. This study is important as it can help improve care and resource allocation in the ICU by better understanding the role of nutrition and frailty in patient outcomes. The study will involve 50 patients admitted to a specific ICU department. Ultrasound, a non-invasive and easy-to-use tool, will be used to measure various indicators of the patients' nutritional status and frailty. This includes measuring the thickness and intensity of muscle echogenicity, particularly in the upper leg muscles like the quadriceps. The study will also record patient demographics, health conditions, lab results, reason and duration of ICU stay, and time needed to wean off mechanical ventilation. Patient frailty will be assessed through interviews using the Clinical Frailty Scale (CFS). The results of these measurements and assessments will be compared to better understand their relationship with patient outcomes.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.50 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Other
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Osijek University Hospital; Medical Faculty
Osijek, CroatiaOpen Osijek University Hospital; Medical Faculty in Google Maps