The Effects of Probiotic Supplementation on Extremely Low Birthweight Infants

October 9, 2018 updated by: Mercy Health System
This is a research study that will look at the effects of giving two nutritional supplements on extremely low birth infants (infants weighing less than 1000 grams or weighing less than approximately 2 lbs 3 1/2 ounces at birth). The nutritional supplements that will be studied are Culturelle for Kids/Culturelle Kids and Align. They are nutritional supplements that each contain a different probiotic. In this study the investigators will mainly be looking at the effect that these supplements may have on how well babies tolerate their feedings and how long they require supplemental intravenous fluids for nutritional support. The investigators will also, however, look at many other factors such as rate of growth, rates of infection, survival rate and the length of time the infant needs to be in the hospital. The investigators will also look at its effect on conditions/complications of prematurity such as bronchopulmonary dysplasia and chronic lung disease (chronic diseases of the lung associated with prematurity), necrotizing enterocolitis and intestinal perforations (serious diseases of the infant's intestines), retinopathy of prematurity (eye disease associated with prematurity), intracranial hemorrhage (bleeding into the brain) and patent ductus arteriosus (a blood vessel connecting two main blood vessels coming out of the heart that does not close spontaneously (by itself).

Study Overview

Detailed Description

The purpose of this research study is to investigate the effect of the administration of the nutritional supplements, Culturelle for Kids/Kids Culturelle in combination with Align, containing the Probiotics Lactobacillus GG and Bifidobacterium Infantis, on feeding tolerance (as determined by the number of days infant is without enteral feedings due to feeding intolerance, number of days infant requires supplemental hyperalimentation/intravenous fluids for nutritional support and number of days to achieve full enteral feedings) in high risk extremely low birth weight infants.

Study Type

Interventional

Enrollment (Actual)

133

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Illinois
      • Rockford, Illinois, United States, 61103
        • Rockford Memorial Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

No older than 2 weeks (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Birthweight between 500-999 grams
  • Apgar score greater than or equal to 3 at 5 minutes
  • Infant free from any known major congenital anomalies or chromosomal/genetic anomalies
  • Infant without any known cyanotic or complex congenital heart disease
  • Infant NPO or on trophic enteral feedings than have been started less than 24 hours previously
  • Infant without prior history of necrotizing enterocolitis or gastrointestinal perforation
  • Infant without previous exposure to probiotics
  • Infant that will be ready to start trophic feedings within the first 14 days of life
  • Infant less than or equal to 14 days of age
  • Infant born to HIV negative mother
  • Written informed consent obtained from mother

Exclusion Criteria:

  • Infant born to HIV positive mother
  • Infant with history of prior probiotic exposure
  • Infant greater than 14 days of age
  • Infant on enteral feedings for greater than 24 hours
  • Infant with major congenital anomaly/chromosomal or genetic anomaly
  • Infant with cyanotic/complex congenital heart disease
  • Infant with previous gastrointestinal perforation/necrotizing enterocolitis
  • 5 minute Apgar score < 3

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Quadruple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Probiotic Supplemented Group
500,000,0000 cells of Lactobacillus GG (utilizing either Culturelle for Kids or Kids Culturelle preparation) and 500,000,000 cells of Bifidobacterium Infantis (utilizing Align capsule) diluted in 3 ml breastmilk/formula and administered enterally from first day of enteral feeds until term gestation/discharge/transfer/death (whichever occurs first) every day infant is receives enteral feedings
Other Names:
  • Align
  • Culture for Kids
  • Kids Culturelle
  • Lactobacillus GG
  • Bifidobacter Infantis
Sham Comparator: Control Group
3 ml enteral feeding of breastmilk/formula administered once daily in addition to regularly prescribed enteral feedings from day of first feeding until term gestation/discharge/transfer/death (which ever occurs first) and administered every day that infant receives enteral feedings
Other Names:
  • Formula
  • Breastmilk

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Feeding Tolerance
Time Frame: Evaluated on a daily basis until hospital discharge/transfer/death up until one year of age
Feeding Tolerance as determined by the number of days infant is without enteral feedings due to feeding intolerance, number of days infant requires supplemental hyperalimentation/intravenous fluids for nutritional support and number of days to achieve full enteral feedings
Evaluated on a daily basis until hospital discharge/transfer/death up until one year of age

Secondary Outcome Measures

Outcome Measure
Time Frame
Necrotizing Enterocolitis (Bell's Stage 2 or greater)
Time Frame: Infants entire inpatient record assessed at/after time of hospital discharge/transfer/death up until 1 year of age
Infants entire inpatient record assessed at/after time of hospital discharge/transfer/death up until 1 year of age
Culture proven sepsis without Necrotizing Enterocolitis
Time Frame: Infants entire inpatient record assessed at/after time of hospital discharge/transfer/death up until one year of age
Infants entire inpatient record assessed at/after time of hospital discharge/transfer/death up until one year of age
Chronic Lung Disease
Time Frame: Infants entire inpatient record assessed at/after time of hospital discharge/transfer/death up until one year of age
Infants entire inpatient record assessed at/after time of hospital discharge/transfer/death up until one year of age
Periventricular Leukomalacia
Time Frame: Infant's entire inpatient record assessed at/after time of hospital discharge/transfer/death up until one year of age
Infant's entire inpatient record assessed at/after time of hospital discharge/transfer/death up until one year of age
Mortality
Time Frame: Infant's entire inpatient record assessed at/after time of hospital discharge/transfer/death up until one year of age
Infant's entire inpatient record assessed at/after time of hospital discharge/transfer/death up until one year of age
Intraventricular Hemorrhage
Time Frame: Infants entire inpatient record assessed at/after time of hospital discharge/transfer/death up until one year of age
Infants entire inpatient record assessed at/after time of hospital discharge/transfer/death up until one year of age
Daily weight gain in grams
Time Frame: Measured daily until time of hospital discharge/transfer/death up until one year of age
Measured daily until time of hospital discharge/transfer/death up until one year of age
Discharge weight measured and expressed by percentile of growth for age
Time Frame: Assessed at the time of discharge/transfer/death up until one year of age
Assessed at the time of discharge/transfer/death up until one year of age
Length of Stay
Time Frame: Measured at time of discharge/transfer/death up until one year of age
Measured at time of discharge/transfer/death up until one year of age

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Kim M Schmidt, MS, APN, NNP, Mercy Health System

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2012

Primary Completion (Actual)

July 11, 2018

Study Completion (Actual)

July 11, 2018

Study Registration Dates

First Submitted

February 4, 2013

First Submitted That Met QC Criteria

February 7, 2013

First Posted (Estimate)

February 11, 2013

Study Record Updates

Last Update Posted (Actual)

October 11, 2018

Last Update Submitted That Met QC Criteria

October 9, 2018

Last Verified

April 1, 2017

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • pROBIOTICS11

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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