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Prophylactic Probiotics to Extremely Low Birth Weight Prematures (PROPEL)

Primary Purpose

Feeding; Difficult, Newborn, Growth Failure, Necrotizing Enterocolitis

Status
Completed
Phase
Phase 2
Locations
Sweden
Study Type
Interventional
Intervention
Lactobacillus reuteri
Placebo
Sponsored by
Ostergotland County Council, Sweden
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Feeding; Difficult, Newborn focused on measuring Probiotics, Lactobacillus reuteri, Prematures, Enteral feeding, Motility, Necrotizing enterocolitis, Sepsis, Weight

Eligibility Criteria

1 Day - 3 Days (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Birth weight < 1000 g
  • Gestational age: v23+0-V27 +6.
  • Age < 72 hours at inclusion.
  • Signed informed consent by parents.

Exclusion Criteria:

  • Fatal or complex congenital malformation at inclusion time.
  • Chromosomal defect at inclusion time.
  • No realistic hope of survival at inclusion time.
  • Gastrointestinal malformation at inclusion time.
  • Participation in another study which aims to influence nutrition, growth, feeding tolerance or necrotizing enterocolitis.

Sites / Locations

  • Vrinnevi Hospital in Norrköping
  • Karolinska

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Lactobacillus reuteri

Placebo

Arm Description

Lactobacillus reuteri DSM 17938, 125 million bacteria/day

The same oil drops as the active study product but without Lactobacillus reuteri

Outcomes

Primary Outcome Measures

Time to Establish Full Enteral Feeds
The age of the infants in days when the infant receive 150 ml/kg/day via enteral feeding for the first time.

Secondary Outcome Measures

Days With Halted Feeding Due to Food Intolerance
Episode with food intolerance. Retention volume> food volume given the last 2 hours (retention checked routinely every 4 hours) and/or clinical signs consistent with necrotizing enterocolitis (reduced general condition and inflated abdomen). The number of such events will also be indicated.
Number of Stools
Time Until Birth Weight is Regained. Specifies the Number of Full Days the Child Has Lived.
Specifies the number of full days the child has lived.
Weight Gain (SD)
In this analysis, the difference in standard deviation score (delta z-scores) for weight, height and head circumference at birth and 14 and 28 days and gestational week 36+0 will be calculated. At gestational week 36+0 also absolute values will be analyzed. A positive delta z-score indicates faster growth than the growth chart would predict.
Mortality
Necrotizing Enterocolitis
Bell´s criteria II-III
Sepsis
Blood culture positive sepsis
Bronchopulmonary Dysplasia
Need of oxygen or CPAP/ventilator at gw 36+0
Weight Gain (SD)
In this analysis, the difference in standard deviation score (delta z-scores) for weight, height and head circumference at birth and 14 and 28 days and gestational week 36+0 will be calculated. At gestational week 36+0 also absolute values will be analyzed. A positive delta z-score indicates faster growth than the growth chart would predict.
Weight Gain (SD)
In this analysis, the difference in standard deviation score (delta z-scores) for weight, height and head circumference at birth and 14 and 28 days and gestational week 36+0 will be calculated. At gestational week 36+0 also absolute values will be analyzed. A positive delta z-score indicates faster growth than the growth chart would predict.
Length Gain (SD)
In this analysis, the difference in standard deviation score (delta z-scores) for weight, height and head circumference at birth and 14 and 28 days and gestational week 36+0 will be calculated. At gestational week 36+0 also absolute values will be analyzed. A positive delta z-score indicates faster growth than the growth chart would predict.
Length Gain (SD)
In this analysis, the difference in standard deviation score (delta z-scores) for weight, height and head circumference at birth and 14 and 28 days and gestational week 36+0 will be calculated. At gestational week 36+0 also absolute values will be analyzed. A positive delta z-score indicates faster growth than the growth chart would predict.
Length Gain (SD)
In this analysis, the difference in standard deviation score (delta z-scores) for weight, height and head circumference at birth and 14 and 28 days and gestational week 36+0 will be calculated. At gestational week 36+0 also absolute values will be analyzed. A positive delta z-score indicates faster growth than the growth chart would predict.
Head Circumference Growth (SD)
In this analysis, the difference in standard deviation score (delta z-scores) for weight, height and head circumference at birth and 14 and 28 days and gestational week 36+0 will be calculated. At gestational week 36+0 also absolute values will be analyzed. A positive delta z-score indicates faster growth than the growth chart would predict.
Head Circumference Growth (SD)
In this analysis, the difference in standard deviation score (delta z-scores) for weight, height and head circumference at birth and 14 and 28 days and gestational week 36+0 will be calculated. At gestational week 36+0 also absolute values will be analyzed. A positive delta z-score indicates faster growth than the growth chart would predict.
Head Circumference Growth (SD)
In this analysis, the difference in standard deviation score (delta z-scores) for weight, height and head circumference at birth and 14 and 28 days and gestational week 36+0 will be calculated. At gestational week 36+0 also absolute values will be analyzed. A positive delta z-score indicates faster growth than the growth chart would predict.
Neurological Development
Bayleys´s test by psychologist
Neurological Development Impairment
A composite of several outcomes: impaired cognition at the Bayleys´test, cerebral palsy, blindness and deafness, divided into normal, mild, moderate and severe. Mild -1SD to -2SD, Moderate <-2D to 3 SD and Severe <3SD

Full Information

First Posted
May 18, 2012
Last Updated
December 12, 2022
Sponsor
Ostergotland County Council, Sweden
Collaborators
BioGaia AB, Ekhaga Foundation, Sweden, Medical Research Council of Southeast Sweden, University Hospital, Linkoeping, The Swedish Research Council, The Swedish Society of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT01603368
Brief Title
Prophylactic Probiotics to Extremely Low Birth Weight Prematures
Acronym
PROPEL
Official Title
Prophylactic Probiotics to Extremely Low Birth Weight Prematures
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Completed
Study Start Date
June 2012 (Actual)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ostergotland County Council, Sweden
Collaborators
BioGaia AB, Ekhaga Foundation, Sweden, Medical Research Council of Southeast Sweden, University Hospital, Linkoeping, The Swedish Research Council, The Swedish Society of Medicine

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Mortality and incidence of severe complications is still high among extremely premature infants. Common causes of severe complications in this population are poor nutrition, necrotizing enterocolitis, and severe infections. Feeding intolerance is also a common problem resulting in prolonged need for intravenous lines and poor nutrition. The aim of the study is to evaluate whether supplementation with the probiotic bacterium Lactobacillus reuteri DSM 17938 daily to premature infants with extremely low birth weight increases feeding tolerance to breast milk and thereby improves nutrition, increases growth and reduces serious complications and mortality in this population. Beyond this, possible mechanisms underlying these effects will be analyzed in stool, breast milk and blood samples.
Detailed Description
RATIONALE Mortality and incidence of severe complications is still high among extremely premature infants. Common causes of severe complications in this population are poor nutrition, necrotizing enterocolitis (NEC), and severe infections. Feeding intolerance is also a common problem resulting in prolonged need for intravenous lines and poor nutrition. There is scientific evidence that dietary supplements with probiotics may have an effect on these manifestations. Lactobacillus reuteri is a well studied probiotic bacterium that has been tested in several clinical studies in premature infants and older children, and the results of these studies and animal studies suggest that this bacterium may also have an effect on growth and mortality in extremely premature infants. Lactobacillus reuteri reduces colonization with pathogenic microbes, stimulates gastric and intestinal motility and shortens hospital stay in moderately premature infants. In animal models, L. reuteri also induces anti-inflammatory immune responses, reduces the symptoms of inflammatory bowel disease and the incidence of NEC. Administration of L. reuteri also improves the intestinal barrier both in human studies in children and in animal studies. Dietary supplements of L. reuteri to extremely premature infants may therefore improve feeding tolerance and nutrition and reduce the incidence of severe complications in this population. HYPOTHESIS Premature infants with extremely low birth weight receiving daily supplements of Lactobacillus reuteri DSM 17938 will reach full enteral feeding faster compared with children receiving placebo. STUDY DESIGN This study will be conducted as a prospective multi-center double blind placebo-controlled study in neonatal intensive care units in Sweden. In total 134 neonates with extremely low birth weight (<1000g) and gestational age <28+0 weeks will be randomized to receive either dietary supplements of Lactobacillus reuteri or placebo. Study product will be identical to the active and placebo group besides the addition of Lactobacillus reuteri (1.25 x 100 million bacteria=0.2 ml oil drops per day) in the active group. The supplementation will commence within 1-3 days after birth and will be given daily until gestational week 36+0. The infants will be followed until gestational week 36+0 and data on feeding tolerance, nutrition, growth, infections, NEC, bronchopulmonary dysplasia, death, and potential confounders will be entered in an individual study protocol. Stool, breast milk, and blood samples will be collected for analyses of possible underlying mechanisms. A 2-year follow up including examination by pediatrician, growth parameters, questionnaire and psychology testing (Bayley´s test) will be performed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Feeding; Difficult, Newborn, Growth Failure, Necrotizing Enterocolitis, Sepsis
Keywords
Probiotics, Lactobacillus reuteri, Prematures, Enteral feeding, Motility, Necrotizing enterocolitis, Sepsis, Weight

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
134 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Lactobacillus reuteri
Arm Type
Active Comparator
Arm Description
Lactobacillus reuteri DSM 17938, 125 million bacteria/day
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
The same oil drops as the active study product but without Lactobacillus reuteri
Intervention Type
Dietary Supplement
Intervention Name(s)
Lactobacillus reuteri
Intervention Description
Oil drops with Lactobacillus reuteri DSM 17938, 125 million bacteria=0.2 ml per day
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Oil drops without Lactobacillus reuteri
Primary Outcome Measure Information:
Title
Time to Establish Full Enteral Feeds
Description
The age of the infants in days when the infant receive 150 ml/kg/day via enteral feeding for the first time.
Time Frame
Birth to gestational week 36+0
Secondary Outcome Measure Information:
Title
Days With Halted Feeding Due to Food Intolerance
Description
Episode with food intolerance. Retention volume> food volume given the last 2 hours (retention checked routinely every 4 hours) and/or clinical signs consistent with necrotizing enterocolitis (reduced general condition and inflated abdomen). The number of such events will also be indicated.
Time Frame
Birth to gestational week 36
Title
Number of Stools
Time Frame
Recorded over the first four weeks
Title
Time Until Birth Weight is Regained. Specifies the Number of Full Days the Child Has Lived.
Description
Specifies the number of full days the child has lived.
Time Frame
Birth to gw 36+0
Title
Weight Gain (SD)
Description
In this analysis, the difference in standard deviation score (delta z-scores) for weight, height and head circumference at birth and 14 and 28 days and gestational week 36+0 will be calculated. At gestational week 36+0 also absolute values will be analyzed. A positive delta z-score indicates faster growth than the growth chart would predict.
Time Frame
At 14th day of life
Title
Mortality
Time Frame
Birth to gw 36+0
Title
Necrotizing Enterocolitis
Description
Bell´s criteria II-III
Time Frame
Birth to gw 36+0
Title
Sepsis
Description
Blood culture positive sepsis
Time Frame
Birth to gw 36+0
Title
Bronchopulmonary Dysplasia
Description
Need of oxygen or CPAP/ventilator at gw 36+0
Time Frame
Gw 36+0
Title
Weight Gain (SD)
Description
In this analysis, the difference in standard deviation score (delta z-scores) for weight, height and head circumference at birth and 14 and 28 days and gestational week 36+0 will be calculated. At gestational week 36+0 also absolute values will be analyzed. A positive delta z-score indicates faster growth than the growth chart would predict.
Time Frame
At 28th day of life
Title
Weight Gain (SD)
Description
In this analysis, the difference in standard deviation score (delta z-scores) for weight, height and head circumference at birth and 14 and 28 days and gestational week 36+0 will be calculated. At gestational week 36+0 also absolute values will be analyzed. A positive delta z-score indicates faster growth than the growth chart would predict.
Time Frame
At gestational week 36+0
Title
Length Gain (SD)
Description
In this analysis, the difference in standard deviation score (delta z-scores) for weight, height and head circumference at birth and 14 and 28 days and gestational week 36+0 will be calculated. At gestational week 36+0 also absolute values will be analyzed. A positive delta z-score indicates faster growth than the growth chart would predict.
Time Frame
At 14th day of life
Title
Length Gain (SD)
Description
In this analysis, the difference in standard deviation score (delta z-scores) for weight, height and head circumference at birth and 14 and 28 days and gestational week 36+0 will be calculated. At gestational week 36+0 also absolute values will be analyzed. A positive delta z-score indicates faster growth than the growth chart would predict.
Time Frame
At 28th day of life
Title
Length Gain (SD)
Description
In this analysis, the difference in standard deviation score (delta z-scores) for weight, height and head circumference at birth and 14 and 28 days and gestational week 36+0 will be calculated. At gestational week 36+0 also absolute values will be analyzed. A positive delta z-score indicates faster growth than the growth chart would predict.
Time Frame
At gestational week 36+0
Title
Head Circumference Growth (SD)
Description
In this analysis, the difference in standard deviation score (delta z-scores) for weight, height and head circumference at birth and 14 and 28 days and gestational week 36+0 will be calculated. At gestational week 36+0 also absolute values will be analyzed. A positive delta z-score indicates faster growth than the growth chart would predict.
Time Frame
At 14th day of life
Title
Head Circumference Growth (SD)
Description
In this analysis, the difference in standard deviation score (delta z-scores) for weight, height and head circumference at birth and 14 and 28 days and gestational week 36+0 will be calculated. At gestational week 36+0 also absolute values will be analyzed. A positive delta z-score indicates faster growth than the growth chart would predict.
Time Frame
At 28th day of life
Title
Head Circumference Growth (SD)
Description
In this analysis, the difference in standard deviation score (delta z-scores) for weight, height and head circumference at birth and 14 and 28 days and gestational week 36+0 will be calculated. At gestational week 36+0 also absolute values will be analyzed. A positive delta z-score indicates faster growth than the growth chart would predict.
Time Frame
At gestational week 36+0
Title
Neurological Development
Description
Bayleys´s test by psychologist
Time Frame
At 2 years corrected age
Title
Neurological Development Impairment
Description
A composite of several outcomes: impaired cognition at the Bayleys´test, cerebral palsy, blindness and deafness, divided into normal, mild, moderate and severe. Mild -1SD to -2SD, Moderate <-2D to 3 SD and Severe <3SD
Time Frame
At 2 years corrected age

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
3 Days
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Birth weight < 1000 g Gestational age: v23+0-V27 +6. Age < 72 hours at inclusion. Signed informed consent by parents. Exclusion Criteria: Fatal or complex congenital malformation at inclusion time. Chromosomal defect at inclusion time. No realistic hope of survival at inclusion time. Gastrointestinal malformation at inclusion time. Participation in another study which aims to influence nutrition, growth, feeding tolerance or necrotizing enterocolitis.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thomas Abrahamsson, MD, PhD
Organizational Affiliation
Linköping University Hospital; County Council of Östergötland
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vrinnevi Hospital in Norrköping
City
Norrköping
ZIP/Postal Code
60379
Country
Sweden
Facility Name
Karolinska
City
Stockholm
ZIP/Postal Code
SE-171 76
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
33923278
Citation
Spreckels JE, Wejryd E, Marchini G, Jonsson B, de Vries DH, Jenmalm MC, Landberg E, Sverremark-Ekstrom E, Marti M, Abrahamsson T. Lactobacillus reuteri Colonisation of Extremely Preterm Infants in a Randomised Placebo-Controlled Trial. Microorganisms. 2021 Apr 24;9(5):915. doi: 10.3390/microorganisms9050915.
Results Reference
derived
PubMed Identifier
33763652
Citation
Marti M, Spreckels JE, Ranasinghe PD, Wejryd E, Marchini G, Sverremark-Ekstrom E, Jenmalm MC, Abrahamsson T. Effects of Lactobacillus reuteri supplementation on the gut microbiota in extremely preterm infants in a randomized placebo-controlled trial. Cell Rep Med. 2021 Feb 22;2(3):100206. doi: 10.1016/j.xcrm.2021.100206. eCollection 2021 Mar 16.
Results Reference
derived

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Prophylactic Probiotics to Extremely Low Birth Weight Prematures

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