Recruiting

Ultrasound Assessment of Nutritional Status and Frailty in Surgical ICU Patients

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Study Aim

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.

What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Frailty

+ Pathologic Processes

+ Pathological Conditions, Signs and Symptoms

Over 18 Years
+4 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Other

Utilizing specific methods not covered by standard models in order to address unique research questions.
Observational
Study Start: February 2026
See protocol details

Summary

Principal SponsorOsijek University Hospital
Study ContactSlavica Kvolik, prof.More contacts
Last updated: March 17, 2026
Sourced from a government-validated database.Claim as a partner

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.

Official TitleUltrasound Indicators of Nutritional Status and Treatment Outcomes in Surgical Patients in the Intensive Care Unit
Principal SponsorOsijek University Hospital
Study ContactSlavica Kvolik, prof.More contacts
Last updated: March 17, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

50 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Other

Some studies use unique or mixed approaches that don't fit standard categories. These may include innovative observational methods or studies tailored to specific research questions.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

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

FrailtyPathologic ProcessesPathological Conditions, Signs and Symptoms

Criteria

1 inclusion criteria required to participate
postoperative intensive care

3 exclusion criteria prevent from participating
surgery of the right leg

paraplegia, tetraplegia

refusal of the patient/guardian to participate in the research (informed consent not signed)

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

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

Recruiting

Osijek University Hospital; Medical Faculty

Osijek, CroatiaOpen Osijek University Hospital; Medical Faculty in Google Maps
Recruiting
One Study Center