Efficacy of Nasojejunal Enteral Feeding in Critically Ill Patients.

Melbourne Health

Status: Completed

Conditions: Critically Ill

Treatments: Procedure: Nasojejunal feeding

Study type: Interventional

Funder types: Other

Identifiers

NCT00256048

2002.228

Details and patient eligibility

About

The purpose of this study is to determine if naso-jejunal feeding (feeding beyond the stomach) improves the efficacy of enteral feeding (feeding into the gut) in critically ill patients.

The study hypothesis is that in patients who fail to establish enteral feeding via the nasogastric route, introduction of nasojejunal feeding will lead to more effective enteral feeding than the current regime involving staged introduction of promotility agents.

Full description

The study examines the area of enteral feeding in critically ill patients. Current standard enteral feeding practice is via a nasogastric with the addition of promotility agents for patients who fail to absorb their enteral nutrition.

This study compares the efficacy of nasojejunal feeding feeding with nasogastric enteral feeding with the addition of promotility agents.

The duration of feeding will be determined by the patients nutritional requirements and their general condition. However the data will be collected for duration of enteral feeding, 28 days or ICU discharge whichever occurs first.

Enrollment: 50 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Adult patients (18years or over) admitted to the ICU with an expected stay of more than 48 hours.

2. Patients commenced on enteral feeding via a nasogastric tube who fail to tolerate gastric feeding due to excessive gastric aspirate volumes.

3. Patients who consent or if the patient is incompetent, the next of kin, who consent, to inclusion in the study.

Exclusion criteria

1. patients less than 18 years of age.
2. Patients with known allergy to promotility agents, metoclopramide or erythromycin.
3. Patients with a contra indication to nasojejunal feeding. -

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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50 participants in 2 patient groups

Standard Care

No Intervention group

Description:

Patients will receive enteral nutrition via a nasogastric tube as per standard feeding regime

Nasojejunal Arm

Active Comparator group

Description:

Patient will receive feeding via a nasojejunal feeding tube

Treatment:

Procedure: Nasojejunal feeding