跳至主要内容
临床试验/NCT07163286
NCT07163286进行中(未招募)不适用

Evaluation and Comparison of Malnutrition and Sarcopenia Risk Using PG-SGA, MUST, Nutriscore, and GLIM Criteria in Cancer Patients Undergoing Chemotherapy

Çanakkale Onsekiz Mart University1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2025年7月1日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
200
试验地点
1
主要终点
PG-SGA short form values

研究概览

简要总结

The study will include approximately 150 adult outpatients diagnosed with solid tumors who are currently receiving chemotherapy. Both early and advanced stage patients of any sex aged 18 and older will be included, provided they are clinically stable and able to participate in the assessments.

详细描述

Background: Malnutrition and sarcopenia are prevalent and clinically significant conditions in cancer patients receiving chemotherapy. Accurate nutritional screening and early diagnosis of sarcopenia are critical for improving treatment outcomes and quality of life. Several screening tools are used for nutritional risk assessment in oncology, including PG-SGA, MUST, Nutriscore, and the recently proposed GLIM criteria.

Objective

This cross-sectional study aims to evaluate the risk of malnutrition and sarcopenia in solid tumor outpatients receiving chemotherapy. It compares the effectiveness and correlation of PG-SGA, MUST, Nutriscore, and GLIM criteria, and investigates their association with sarcopenia, measured via handgrip strength and CT-based skeletal muscle index at the L3 level.

Methods: Approximately 150 adult cancer patients receiving active outpatient chemotherapy will be assessed. Nutritional status will be evaluated using PG-SGA, MUST, Nutriscore, and GLIM. Sarcopenia will be determined via handgrip strength testing and analysis of CT images. Charlson Comorbidity Index will be used to assess comorbidity burden.

研究设计

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

入排标准

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

入选标准

  • Age ≥ 18 years
  • Diagnosed with a solid tumor (e.g., breast, lung, GI, gynecologic cancers)
  • Receiving active outpatient chemotherapy
  • Recent abdominal CT scan within the last 3 months or planned
  • Provided written informed consent
  • Physically and mentally able to complete study procedures

排除标准

  • Declined or unable to give informed consent
  • Cognitive impairment or mental status preventing participation
  • Neuromuscular diseases affecting muscle mass (e.g., myopathy, MND, severe neuropathy)
  • Inadequate CT image quality for L3 analysis
  • Acute infection or illness within the past month
  • Upper limb deformity or severe pain preventing handgrip testing
  • Incomplete assessments or withdrawal of consent during the study

结局指标

主要结局

PG-SGA short form values

时间窗: From enrollment to 6 month

Nutriscore

时间窗: From enrollment to 6 month

次要结局

未报告次要终点

研究者

发起方
Çanakkale Onsekiz Mart University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Şeyma Eroğlu

Oncology Fellowship Dr.

Çanakkale Onsekiz Mart University

研究点 (1)

Loading locations...

相似试验