MedPath

Evaluation of Predictive Visual Analog Scale (VAS) for Determining the Ingesta of Patients Carrying a Digestive Cancer

Completed
Conditions
Digestive System Neoplasms
Registration Number
NCT02781532
Lead Sponsor
Centre Hospitalier Universitaire de Nice
Brief Summary

The main objective of our study is to determine if the evaluation of ingesta of cancer patients by VAS (on the day of hospitalization) is able to predict the actual ingesta of patients during hospitalization (for patients malnourished, at risk of malnutrition or risk free).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Patients aged over 18 years
  • Admitted to hospital for systemic therapy of gastrointestinal cancer
  • Signature of the non-opposition.
Exclusion Criteria
  • Patients who because of their affection will fasted more than 12:00 during the three days preceding hospitalization.
  • Artificial nutrition Patients

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Evaluation of ingesta3 days

Evaluation of ingesta will be done using SAV scale.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

CHU de Nice

🇫🇷

France, France

© Copyright 2025. All Rights Reserved by MedPath