Tolerance of Increased Infusion Rates of Intravenous Fat Emulsions in Very Low Birth Weight Infants

This study has been completed.

First Received: June 19, 2008 Last Updated: June 23, 2008 History of Changes

Sponsored by:	OSF Saint Francis Medical Center
Information provided by:	OSF Saint Francis Medical Center
ClinicalTrials.gov Identifier:	NCT00702767

Purpose

This study was completed in October 2006. No further participates are being recruited.

Condition	Intervention
Low Birth Weight	Drug: INTRALIPIDS

Study Type:	Interventional
Study Design:	Treatment, Randomized, Open Label, Parallel Assignment
Official Title:	Tolerance of Increased Infusion Rates of Intravenous Fat Emulsions in Very Low Birth Weight Infants During the First Week of Life

Further study details as provided by OSF Saint Francis Medical Center:

Enrollment:	110
Study Start Date:	July 2005
Study Completion Date:	April 2007
Primary Completion Date:	October 2006 (Final data collection date for primary outcome measure)

Intervention Details:

INTRAVENOUS FAT EMULSIONS

Eligibility

Criteria

Inclusion Criteria:

All infants who are Appropriate for Gestational Age at Birth and who have a birthweight between 750-1500 grams will be enrolled in this study.

Contacts and Locations

No Contacts or Locations Provided

More Information

No publications provided

Responsible Party:	Children's Hospital of Illinois at OSF-Saint Francis Medical Center ( Dr. Kamlesh S. Macwan, Neonatalogist )
Study ID Numbers:	05-060
Study First Received:	June 19, 2008
Last Updated:	June 23, 2008
ClinicalTrials.gov Identifier:	NCT00702767 History of Changes
Health Authority:	United States: Institutional Review Board

Keywords provided by OSF Saint Francis Medical Center:

This study was completed in October 2006

Study placed in the following topic categories:

Body Weight
Birth Weight
Signs and Symptoms

Additional relevant MeSH terms:

Body Weight
Birth Weight
Signs and Symptoms

ClinicalTrials.gov processed this record on May 07, 2009