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NCT00702767 Clinical Trial

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

Low Birth Weight Clinical Trial

Official title:
Tolerance of Increased Infusion Rates of Intravenous Fat Emulsions in Very Low Birth Weight Infants During the First Week of Life

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00702767
Other study ID # 05-060
Secondary ID
Status Completed
Phase N/A
First received June 19, 2008
Last updated June 23, 2008
Start date July 2005
Est. completion date April 2007

Study information
Verified date June 2008
Source OSF Healthcare System
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

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

Recruitment information / eligibility
Status Completed
Enrollment 110
Est. completion date April 2007
Est. primary completion date October 2006
Accepts healthy volunteers No
Gender Both
Age group N/A to 1 Day
Eligibility 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.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• INTRALIPIDS
INTRAVENOUS FAT EMULSIONS

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
OSF Healthcare System
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