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临床试验/NCT06590350
NCT06590350
进行中(未招募)
不适用

Individualized NUTRItional RISK and Oriented Nutritional Support

Fondazione Policlinico Universitario Agostino Gemelli IRCCS1 个研究点 分布在 1 个国家目标入组 100 人2024年6月4日
适应症Malnutrition

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
Malnutrition
发起方
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
入组人数
100
试验地点
1
主要终点
Difference in the duration of hospitalization
状态
进行中(未招募)
最后更新
8个月前

概览

简要总结

The objective of this study is to evaluate whether, in patients who are given early nutritional counseling, there is a reduction in the length of hospitalization and the rate of nosocomial infections, resulting in a decrease in inpatient costs, compared with patients who do not benefit from this intervention.

详细描述

Patients admitted-from the date following the date of approval of the protocol for the following 12 months-will be enrolled at the Departmental Simple Operating Unit Admission Room of the Policlinico Universitario A. Gemelli and who have undergone NRS-2002 screening. Data only of patients with NRS-2002 \>3 admitted will be considered and extracted via the Foundation's computer system (Trackcare). Patients will have been managed by caregivers who spontaneously requested (as is the case to date) nutritional counseling. Therefore, the study will not change current clinical practice. Two cohorts will be drawn and formed and compared: * Cohort 1: patients at risk of malnutrition (NRS-2002 ≥3) who received clinical nutrition counseling within 72 hours of ward admission * Cohort 2: the patients at risk of malnutrition (NRS-2002 ≥3) who did NOT receive clinical nutrition counseling beyond 72 hours after ward admission. At present, at Fondazione Policlinico Universitario A. Gemelli, the Clinical Nutrition Unit is approached on an ad hoc basis by the individual ward attending physician, without a specific procedure: the physician calls in Clinical Nutrition specialists for consultation if in his or her judgment the patient needs nutritional support. The mode of formation of the two cohorts will be entirely spontaneous, that is, according to current clinical practice, given by the judgment of the ward treating physician. In a spontaneous manner, two cohorts will be formed among patients at risk of malnutrition (NRS-2002≥3), one of which will have received specialized nutritional support within 72 hours, the other will not. Only patients 'at risk of malnutrition' will be tracked, highlighting outcomes among those in this category who received the targeted intervention at the appropriate times, versus those who did not. The enrollment department is the same for all patients. es, versus those who did not. The enrollment department is the same for all patients.

注册库
clinicaltrials.gov
开始日期
2024年6月4日
结束日期
2025年10月1日
最后更新
8个月前
研究类型
Observational
性别
All

研究者

入排标准

入选标准

  • Age \>18 years
  • NRS-2002 ≥3
  • Length of stay \> 4 days
  • Informed consent to participate in the study

排除标准

  • NRS-2002 \<3
  • Length of stay \< or = 4 days
  • Absence of informed consent

结局指标

主要结局

Difference in the duration of hospitalization

时间窗: 12 months

Difference in the overall length of stay in patients at risk of malnutrition (NRS-2002 ≥ 3) who received nutrition counseling within 72 hours of ward admission compared to the group of patients at risk who did not receive counseling within 72 hours.

次要结局

  • Differences in the number of infectious complications(12 months)
  • Frequency of adherence to diet and AFMS proposed at visit(12 months)
  • Differences in hospitalization costs for the healthcare(12 months)

研究点 (1)

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