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临床试验/NCT07409519
NCT07409519招募中不适用

Nutritional Screening in Patients With Cardiovascular Disease

Hull University Teaching Hospitals NHS Trust1 个研究点 分布在 1 个国家目标入组 250 人开始时间: 2025年8月20日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
250
试验地点
1
主要终点
Time in ICU

研究概览

简要总结

This is a nutritional screening and assessment study conducted prior to heart surgery. The nutritional status of patients will be assessed by a series of questionnaires, blood/urine biomarkers and measurement of grip strength and body composition. The investigators will then evaluate of any of the assessments are linked with clinical outcomes following surgery. For example, how long do patients stop in the intensive care unit (ICU), in hospital and how many complications patients experience.

The investigators hope to use this important clinical data to understand how medical staff can identify a poor nutritional status and which patients may need nutritional support prior to surgery.

详细描述

This is a cross sectional nutritional screening and assessment study conducted prior to cardiac surgery . The investigators will focus on comparing aspects of nutritional status with robust and validated clinical outcomes (mechanical ventilation, ICU time, hospital stay and Society of Cardiothoracic Surgery (SCTS) complications). The investigators will utilise various nutritional screening questionnaires and assessments, including routine clinical malnutrition tools (i.e. MUST, NRS), plus more nutritional quality assessments such as the NOVA ultra-processed food intake, mediterranean diet and blood biomarker panels such as the Prognostic Nutritional Index (PNI), Controlling Nutritional Status (CONUT).

The investigators will also undertake a functional grip strength test and measure body composition including fat mass (FM) & fat-free mass (FFM), segmental analysis, sarcopenic obesity and visceral fat. The study will also conduct questionnaires regarding other lifestyle related factors (sleep, recent physical activity, stress, anxiety, depression) which might also influence surgical outcomes.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Cross Sectional

入排标准

年龄范围
40 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • No pre-specified inclusion criteria to ensure we recruit a representative group of patients.

排除标准

  • All patients without proficiency in English that allows completion of questionnaires
  • Unable to provide written consent

研究组 & 干预措施

Surgical- Group 1

干预措施: Nutritional Screening (Behavioral)

结局指标

主要结局

Time in ICU

时间窗: From ICU admission until ICU discharge, up to 30 days

The total time in hours spent in the ICU, calculated from ICU admission following cardiac surgery to ICU discharge to the general cardiology ward

Complications post cardiac surgery

时间窗: Number of complications following cardiac surgery, up to 30 days

The number of Society of Cardio-thoracic Surgery register of complications

Length of Hospital Stay

时间窗: From hospital admission until hospital discharge, up to 30 days

Length of hospital stay from admission to medical discharge

次要结局

未报告次要终点

研究者

申办方类型
Other Gov
责任方
Sponsor

研究点 (1)

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