Metoclopramide Use in Very Low Birth Weight Newborns

Status Completed

Clinical Trial Summary

During the first 7 days of life very small babies will receive the drug metoclopramide or a salt solution through an intravenous line. They will also begin to receive a very small amount of breast milk or formula within the first 72 hours of life, in addition toother nourishment that is provided by an intravenous line, according to standard hospital procedure. We think that the babies who receive the medication may reach full oral feeds than babies who receive the salt solution.

Clinical Trial Description

Clinically stable, premature babies (birth weight between 500 and 1,250g) will be randomized to receive metoclopramide (0.1 mg/kg IV q8h)or an equal volume of placebo for 7 days.A transition feeding schedule will begin within the first 72 hours of life. The time to full feeds for the 2 groups will be analyzed. ;

Study Design

Related Conditions & MeSH terms

Infant, Premature

Clinical Trial Details

NCT number	NCT00242450
Study type	Interventional
Source	Lawson Health Research Institute
Contact
Status	Completed
Phase	Phase 4
Start date	March 2002
Completion date	July 2005

View Details

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