跳至主要内容
临床试验/NCT07143084
NCT07143084Enrolling By Invitation不适用

Investigation of the Relationship Between Nutritional Status Assessment and Frailty in Critical Care Patients

Ankara Training and Research Hospital1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年5月15日最近更新:
适应症

试验速览

阶段
不适用
状态
Enrolling By Invitation
发起方
入组人数
100
试验地点
1
主要终点
Correlation between CONUT scale and frailty in intensive care patients

研究概览

简要总结

This study aims to understand the effects of these two parameters on clinical outcomes by examining the relationship between NUTRIC and CONUT scores in intensive care patients. The results of the study may contribute to the development of new approaches to the treatment process of patients by better understanding the relationship between nutritional status and pre-hospital frailty in intensive care units. In addition, eliminating the deficiencies in this area will pave the way for the creation of more effective and personalized treatment plans for similar patients.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •48 hours min. ICU stay

排除标准

  • •Patients who are under 65 years of age
  • •whose intensive care stay does not exceed 48 hours
  • •who have missing data for serum albumin or lymphocyte count or total cholesterol,
  • •who have been diagnosed with hematological diseases such as leukemia or lymphoma

结局指标

主要结局

Correlation between CONUT scale and frailty in intensive care patients

时间窗: From enrollment 2 days

To evaluate the correlation between the CONUT scale and frailty, Pearson or Spearman correlation analysis will be performed depending on suitability for normal distribution. Logistic regression analysis will be performed to assess the independent association between CONUT scale and frailty. Potential confounding variables such as age, gender, APACHE II score, and activities of daily living will be included in the regression model.

次要结局

  • Association of NUTRIC score and CONUT scale with clinical outcomes(From enrollment to through study completion an average of 1 year)

研究者

发起方
Ankara Training and Research Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ayşe EKEN

Principal Investigator

Ankara Training and Research Hospital

研究点 (1)

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