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Diarrhea and Stipsis in Critically Ill Patients (NUTRITI)

A

Azienda Sanitaria-Universitaria Integrata di Udine

Status

Completed

Conditions

Diarrhea
Critical Illness
Nutritional Deficiency
Nutritional and Metabolic Disease
Constipation
ICU Acquired Weakness
Enteral Feeding Intolerance

Treatments

Other: ARTIFICIAL NUTRITION

Study type

Observational

Funder types

Other

Identifiers

NCT05473546
NUTRITI

Details and patient eligibility

About

This study prospectively observed the complications intended as diarrhea or sti-sis that critically ill patients developed within 7 days after ICU admission.

In addition, secondary aims investigated through bioimpedenziometry the loss of lean body mass and changes in phase angle during the same period of ICU stay.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ICU ANTICIPATED LENGTH OF STAY > 72 HOURS
  • AGE > 18 YEARS
  • NEED FOR ARTIFICIAL NUTRITION

Exclusion criteria

  • AGE < 18 YEARS
  • ICU ANTICIPATED LENGTH OF STAY < 72 HOURS
  • NO NEED FOR ARTIFICIAL NUTRITION
  • BMI<16 KG/M2

Trial design

100 participants in 1 patient group

CRITICALLY ILL PATIENTS
Description:
ADULTS PATIENTS ADMITTED TO ICU DUE TO ACUTE ILLNESS THAT REQUIRE AT LEAST 72H OF STAY. FOR THE FIRST 7 DAYS OF STAY IN ICU, DATA ABOUT NUTRITIONAL INTERVENTION WILL BE RECORDED SUCH AS: ROUTE OF NUTRITION ADMINISTRATION, AMOUNT OF NUTRITION DELIVERED PER DAY, CALORIC TARGETS, PROTEIN REQUIREMENTS, diarrhea, CONSTIPATION, BIA ANALYSIS.
Treatment:
Other: ARTIFICIAL NUTRITION

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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