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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02781532

Enrollment

100

Registered

2016-05-24

Start date

2014-04-30

Completion date

2015-01-31

Last updated

2016-05-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Digestive System Neoplasms

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).

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

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

Design outcomes

Primary

Measure	Time frame	Description
Evaluation of ingesta	3 days	Evaluation of ingesta will be done using SAV scale.

Countries

France

Outcome results