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OpenTrials
Completed

NCT Number: NCT02781532

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

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).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

CHU de Nice

France, 06000

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. Evaluation of ingesta

    Time frame: 3 days

    Evaluation of ingesta will be done using SAV scale.

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire de Nice

Other

Registry information

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
May 24, 2016
Registry last updated
May 24, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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