Oropharyngeal Colostrum for Immune Stimulation in Very Low Birth Weight Infants
Primary Purpose
Very Low Birth Weight Infants
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
application of mother's own colostrum
application of sterile water
Sponsored by
About this trial
This is an interventional prevention trial for Very Low Birth Weight Infants focused on measuring very low birth weight infants, VLBW infants, colostrum
Eligibility Criteria
Inclusion Criteria:
- infants with a birth weight less than 1500 grams (or 3.3 lbs) born at Penn State Hershey Medical Center and admitted to the PSUCH NICU immediately after birth
Exclusion Criteria:
- Infants with major congenital anomalies or chromosomal syndromes incompatible with life Infants of mothers not willing to provide colostrum for their infant in the first week of life Infants of mothers with known HIV, Hepatitis B or Hepatitis C as these infections may be transmitted through breast milk
Sites / Locations
- Penn State Milton S. Hershey Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Colostrum
Sterile water
Arm Description
Outcomes
Primary Outcome Measures
Change in salivary secretory Ig-A concentration from baseline to 2 weeks of age
Secondary Outcome Measures
time to reach full enteric feeds
day of life when full enteral feeds attained, defined as a volume of 140-150mL/kg/day
episodes of suspected or culture positive sepsis
number of documented septic events either culture proven or those treated with a full course of antibiotics 7-14 days
Full Information
NCT ID
NCT01443091
First Posted
September 26, 2011
Last Updated
May 25, 2017
Sponsor
Milton S. Hershey Medical Center
Collaborators
Children's Miracle Network
1. Study Identification
Unique Protocol Identification Number
NCT01443091
Brief Title
Oropharyngeal Colostrum for Immune Stimulation in Very Low Birth Weight Infants
Official Title
Oropharyngeal Colostrum for Immune Stimulation in Very Low Birth Weight Infants
Study Type
Interventional
2. Study Status
Record Verification Date
April 2015
Overall Recruitment Status
Completed
Study Start Date
January 2011 (undefined)
Primary Completion Date
June 2013 (Actual)
Study Completion Date
December 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Milton S. Hershey Medical Center
Collaborators
Children's Miracle Network
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Colostrum, mothers' early breastmilk, contains multiple factors that provide immune protection to very low birth weight (VLBW) infants, a population at high risk for hospital-acquired infections. However, critical illness during the first few days of life often prevents the initiation of enteral feeds, placing these infants at even higher risk for morbidities including feeding intolerance and infection. Oropharyngeal administration has been proposed as an alternative route of delivery for colostrum and the immune benefits it provides. Research from animal and adult human models supports oropharyngeal administration as a potentially safe and effective mode of delivery for immune therapies. Immune components of colostrum, such as secretory IgA, may have both direct and indirect effects on the immune system. The purpose of this proposed randomized, placebo-controlled pilot study is to determine the effect of oropharyngeally administered colostrum (OAC) on immune stimulation in VLBW infants, as measured by secretory IgA (sIgA) levels. In addition to measuring sIgA response to OAC the investigators will also collect clinical data to determine if OAC has effects on tolerance of enteral feedings and rates of infection. The investigators hypothesize OAC will have a moderate effect on salivary secretory IgA concentration in VLBW infants. If proven efficacious, utilization of OAC in VLBW infants could have far reaching consequences for these highly fragile babies including lower rates of infection, improved tolerance of enteral feedings, and shorter NICU stays.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Very Low Birth Weight Infants
Keywords
very low birth weight infants, VLBW infants, colostrum
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
43 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Colostrum
Arm Type
Experimental
Arm Title
Sterile water
Arm Type
Placebo Comparator
Intervention Type
Other
Intervention Name(s)
application of mother's own colostrum
Intervention Description
application of 0.2mL of mother's own colostrum to the infant's oropharyngeal mucosa every 3 hours for 5 days (day of life 2 until day of life 7)
Intervention Type
Other
Intervention Name(s)
application of sterile water
Intervention Description
application of 0.2mL sterile water to the infant's oropharyngeal mucosa every 3 hours for 5 days (from day of life 2 until day of life 7)
Primary Outcome Measure Information:
Title
Change in salivary secretory Ig-A concentration from baseline to 2 weeks of age
Time Frame
2 weeks of age
Secondary Outcome Measure Information:
Title
time to reach full enteric feeds
Description
day of life when full enteral feeds attained, defined as a volume of 140-150mL/kg/day
Time Frame
first few weeks of age
Title
episodes of suspected or culture positive sepsis
Description
number of documented septic events either culture proven or those treated with a full course of antibiotics 7-14 days
Time Frame
initial hospital stay 1-3 months
10. Eligibility
Sex
All
Maximum Age & Unit of Time
3 Days
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
infants with a birth weight less than 1500 grams (or 3.3 lbs) born at Penn State Hershey Medical Center and admitted to the PSUCH NICU immediately after birth
Exclusion Criteria:
Infants with major congenital anomalies or chromosomal syndromes incompatible with life Infants of mothers not willing to provide colostrum for their infant in the first week of life Infants of mothers with known HIV, Hepatitis B or Hepatitis C as these infections may be transmitted through breast milk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kristen M Glass, MD
Organizational Affiliation
Penn State Milton S. Hershey Medical Center/Penn State College of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Penn State Milton S. Hershey Medical Center
City
Hershey
State/Province
Pennsylvania
ZIP/Postal Code
17033
Country
United States
12. IPD Sharing Statement
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Oropharyngeal Colostrum for Immune Stimulation in Very Low Birth Weight Infants
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