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

Primary Purpose

Low Birth Weight

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
INTRALIPIDS
Sponsored by
OSF Healthcare System
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Low Birth Weight focused on measuring This study was completed in October 2006

Eligibility Criteria

undefined - 1 Day (Child)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Secondary Outcome Measures

    Full Information

    First Posted
    June 19, 2008
    Last Updated
    June 23, 2008
    Sponsor
    OSF Healthcare System
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00702767
    Brief Title
    Tolerance of Increased Infusion Rates of Intravenous Fat Emulsions in Very Low Birth Weight Infants
    Official Title
    Tolerance of Increased Infusion Rates of Intravenous Fat Emulsions in Very Low Birth Weight Infants During the First Week of Life
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2008
    Overall Recruitment Status
    Completed
    Study Start Date
    July 2005 (undefined)
    Primary Completion Date
    October 2006 (Actual)
    Study Completion Date
    April 2007 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    OSF Healthcare System

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

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

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Low Birth Weight
    Keywords
    This study was completed in October 2006

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    110 (Actual)

    8. Arms, Groups, and Interventions

    Intervention Type
    Drug
    Intervention Name(s)
    INTRALIPIDS
    Intervention Description
    INTRAVENOUS FAT EMULSIONS

    10. Eligibility

    Sex
    All
    Maximum Age & Unit of Time
    1 Day
    Accepts Healthy Volunteers
    No
    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.

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    18829797
    Citation
    Drenckpohl D, McConnell C, Gaffney S, Niehaus M, Macwan KS. Randomized trial of very low birth weight infants receiving higher rates of infusion of intravenous fat emulsions during the first week of life. Pediatrics. 2008 Oct;122(4):743-51. doi: 10.1542/peds.2007-2282.
    Results Reference
    derived

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

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