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Analysis of Risk Factors and Prognostic Predictive Value in Sepsis Patients With Nutritional Risk

I

Inner Mongolia Medical University

Status

Completed

Conditions

Nutritional Risk
Sepsis

Treatments

Other: Retrospective data analysis, no intervention

Study type

Observational

Funder types

Other

Identifiers

NCT07278167
AHInnerMongolia-NT

Details and patient eligibility

About

Sepsis is a common critical illness in intensive care units, characterized by systemic inflammatory response, immune dysfunction, microcirculatory issues, and multi-organ failure. These factors lead to high mortality rates and poor prognoses for patients. Nutritional risk is a significant complication in patients with sepsis, with a prevalence of 38% - 78. Sepsis-induced hypermetabolism and hypercatabolism result in increased energy expenditure and accelerated protein breakdown in affected patients, which subsequently exacerbates the risk of malnutrition. Malnutrition weakens immune function, reduces resistance to infections, and impairs immune regulation in sepsis patients. It worsens organ dysfunction, prolongs ICU hospitalization, and increases morbidity and mortality rates. Early identification and intervention for potential risk factors in patients with sepsis, particularly those with nutritional risk, is crucial for enhancing their prognosis. There is a notable lack of sensitive indicators for assessing the prognosis of sepsis patients at nutritional risk. Recent studies have begun exploring physical assessment measures in ICU settings as accessible and noninvasive tools for evaluation. This study aims to investigate the predictive value of nutritional laboratory indicators and physical measurements regarding the 28-day outcomes of ICU patients with sepsis and nutritional risk, providing a foundation for early clinical intervention.

Enrollment

400 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Met the diagnostic criteria for sepsis 3.0
  2. Met the diagnostic criteria for nutritional risk (NRS-2002 score ≥ 3)
  3. ICU stay≥2 days
  4. Age ≥ 18

Exclusion criteria

  1. Edema
  2. Tumor patients
  3. Pregnancy
  4. Lack of complete laboratory results

Trial design

400 participants in 1 patient group

survivors/non-survivors
Treatment:
Other: Retrospective data analysis, no intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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