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Trial registered on ANZCTR


Registration number
ACTRN12622001290785p
Ethics application status
Submitted, not yet approved
Date submitted
19/09/2022
Date registered
4/10/2022
Date last updated
4/10/2022
Date data sharing statement initially provided
4/10/2022
Type of registration
Prospectively registered

Titles & IDs
Public title
Effect of Probiotic dose escalation on faecal microbiota and gut inflammation in extremely preterm infants – A randomised study
Scientific title
Effect of Probiotic dose escalation on faecal microbiota and gut inflammation in extremely preterm infants – A randomised study
Secondary ID [1] 307948 0
Nil known
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Preterm gut inflammation 327603 0
Necrotising enterocolitis 327604 0
Condition category
Condition code
Inflammatory and Immune System 324690 324690 0 0
Other inflammatory or immune system disorders
Oral and Gastrointestinal 324691 324691 0 0
Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Probiotic mixture containing B. breve M-16V, B. longum subsp. infantis M-63, and B. longum subsp. longum BB536 (Total 3 x 10^9 colony forming unit (cfu) (Guaranteed) in one-gram sachets, Manufactured and supplied by Morinaga Milk Industries, Japan).The single dose (1.5×10^9 cfu/day) will be given via the feeding tube until reaching feeds of 50 mL/kg/day. It will be increased thereafter to 3×10^9 (given twice a day in divided doses), 6×10^9 (given twice a day in divided doses) or 9 ×10^9 cfu (given twice a day in divided doses) based on the allocation status of the enrolled infants, once feeds exceed 50 mL/kg/day. Probiotics will be continued until term equivalent age.
Contents of one sachet will be diluted with 2mL sterile water to make a final volume of 3mL reconstituted solution. This reconstituted solution should be administered immediately after reconstitution. This can be given orally or via tube at any time with regards to feeds.
Probiotics dose is charted in the drug chart for administration
Intervention code [1] 324406 0
Prevention
Comparator / control treatment
Group of preterm neonates receiving 3×10^9 (given twice a day in divided doses) shall be the controls.
Control group
Dose comparison

Outcomes
Primary outcome [1] 332507 0
1) Faecal Calprotectin levels.
Timepoint [1] 332507 0
T1: As soon as possible after birth
T2: Four weeks after supplementation
Primary outcome [2] 332564 0
2) Faecal microbiota analysis (composite outcome):(A) Faecal microbiota assessed using 16S ribosomal RNA gene sequencing. (B) Next-generation sequencing.
Timepoint [2] 332564 0
T1: As soon as possible after birth
T2: Four weeks after supplementation
Secondary outcome [1] 413772 0
Time to full feeds of 150 ml/kg/day assessed by medical records
Timepoint [1] 413772 0
Before discharge
Secondary outcome [2] 413936 0
Mental and psychomotor development indices at 24 months of age using Bayley Scale of Infant and Toddler Development (Bayley-III) assessment
Timepoint [2] 413936 0
Developmental assessment: 18 to 24 months
Secondary outcome [3] 414115 0
Necrotising enterocolitis >stage II assessed by radiology and/or intraoperative and/or histopathology finding
Timepoint [3] 414115 0
Before discharge
Secondary outcome [4] 414116 0
All-cause mortality: Data shall be collected from medical records.
Timepoint [4] 414116 0
Before discharge
Secondary outcome [5] 414117 0
Late onset sepsis as assessed by blood culture
Timepoint [5] 414117 0
Before discharge
Secondary outcome [6] 414118 0
Duration of parenteral nutrition: Data shall be collected from medical records
Timepoint [6] 414118 0
Before discharge
Secondary outcome [7] 414119 0
Hospital stay: Data shall be collected from medical records
Timepoint [7] 414119 0
Before discharge
Secondary outcome [8] 414120 0
Anthropometry (Weight, length and head circumference) at discharge. Nurses routinely measure weight, head circumference and length and enter in to medical record. Anthropometry data shall be collected from medical record.
Timepoint [8] 414120 0
Before discharge
Secondary outcome [9] 414121 0
Sepsis due to the administered bifidobacterial strains (Blood culture)
Timepoint [9] 414121 0
Before discharge
Secondary outcome [10] 414122 0
Abdominal distension: Data shall be collected from medical records.
Timepoint [10] 414122 0
Before discharge
Secondary outcome [11] 414123 0
Diarrhoea and vomiting: Data shall be collected fro medical records.
Timepoint [11] 414123 0
Before discharge
Secondary outcome [12] 414124 0
Faecal SCFA levels assessed by modified gas chromatography–mass spectrometry.
Timepoint [12] 414124 0
T1: As soon as possible after birth
T2: 4 weeks after probiotics supplementation

Eligibility
Key inclusion criteria
: (1) gestation of <28 weeks, (2) readiness to commence on feeds or on feeds for <12 hours and (3) informed parental consent.
Minimum age
0 Days
Maximum age
14 Weeks
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
(1) congenital malformations, (2) chromosomal aberrations, (3) not ready for feeds/on feeds for more than equal to 12 hours.

Study design
Purpose of the study
Prevention
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Opaque, sealed and coded envelopes will be used for randomisation. Allocation concealment will be optimised by prescribing allocation only after obtaining informed parental consent and recording basic neonatal data. The clinical trial pharmacist will supply the randomisation sequence and the sachets containing three-strain (B. breve M-16V, B. longum subsp. infantis M-63 and B. longum subsp. longum BB536; 1×10^9 of each strain/g sachet) probiotic manufactured by Morinaga Milk Industry Co., Japan, to the nursing staff.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Group allocation will be based on computer-generated randomisation sequence in random block sizes of 2 and 4.
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?


The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Parallel
Other design features
This will be an open label study. However, all outcome assessors, including microbiology experts assessing the laboratory-based outcomes, and developmental paediatricians assessing growth and neurodevelopment at 24 months of age using Bayley III will be masked to the allocation status of the enrolled infants.
Phase
Not Applicable
Type of endpoint/s
Safety/efficacy
Statistical methods / analysis
Primary outcome
Based on a mean reduction in calprotectin from baseline to 3–4 weeks post-supplementation of 51 µg/g (standard deviation: 133 µg/g) in 13 extremely preterm neonates in the live three-strain probiotic group of a small trial conducted in our unit, a total sample of 75 participants, 25 in each of three dosage groups, achieves 80% power to detect a difference of approximately 27 µg/g between group mean changes from baseline, while adjusting for baseline calprotectin levels. The calculation also allows for a dropout rate of approximately 10%. The sample size calculation was performed with Power Analysis and Sample Size (PASS 2019. NCSS, LLC. Kaysville, Utah, USA).
The microbiome will be compared between the three doses using the methods outlined in the included appendix. Samples from 25 children in each group (50,000 16S reads; ~50M shotgun reads) would have ~80% power to detect the compositional taxonomic difference of gut microbiome at 5% a level. Most of the parametric and non-parametric test (Wilcoxon Rank-Sum Tests) will have 80% power for individual metagenomics markers (e.g. abundance of particular species) given a non-negligible effect size (fold change or Cohen's d) at sample size 25. T-test will be preferred in our analysis by converting the raw variables into normal-distribution variables.
The power of detecting compositional difference between the groups at a given level of type 1 error (5%) depends on two factors— the sample size and the number of reads. The reads number of 50,000 is one of the common throughputs of 16S rRNA sequencing (it corresponds to around 5Gb shotgun metagenomic sequencing). We have used this fixed number of reads in our power evaluation. The number of samples in each group will influence the type 2 error (and power) detecting the compositional differences between two groups based on metagenomic simulations. The number of Monte-Carlo experiments was set to 5000 for each simulated sample.
The approach to bioinformatics analysis will be based on the principle of intention to treat.
Type of variables: (1) Categorical: Presence/absence of particular species or pathways; the clusters based on unsupervised clustering of gut microbial profile, etc. (2) Continuous: Alpha-diversity, richness, abundance of particular species or pathways, or the difference of these numeric variables (treatment vs baseline) etc.
Odds ratio (OR) vs relative risk (RR): The R package "sjstats" and “logisticRR” can be used to calculate the OR and the RR between binary outcomes (e.g. presence/absence of a particular species or a pathway).
Secondary outcomes
Continuous variables will be compared using the t test for normally distributed data and Wilcoxon rank sum test for skewed data. Categorical variables will be compared using the fisher’s exact test. Logistic regression analysis will be used for analysis of binary outcomes (primary outcome) to derive relative risk and 95% confidence intervals (CI). Linear regression analysis will be used for continuous outcomes to derive regression coefficients and respective CI. A p value <0.05 will be considered statistically significant.

Recruitment
Recruitment status
Not yet recruiting
Date of first participant enrolment
Anticipated
2/02/2023
Actual
Date of last participant enrolment
Anticipated
31/12/2023
Actual
Date of last data collection
Anticipated
31/01/2024
Actual
Sample size
Target
75
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
WA
Recruitment hospital [1] 23130 0
King Edward Memorial Hospital - Subiaco
Recruitment postcode(s) [1] 38490 0
6008 - Subiaco

Funding & Sponsors
Funding source category [1] 312215 0
Self funded/Unfunded
Name [1] 312215 0
Country [1] 312215 0
Primary sponsor type
Government body
Name
Child and adoloscent health service
Address
Department of Neonatology
King Edward memorial Hospital
374 Bagot Road
Subiaco 6008
Western Australia
Country
Australia
Secondary sponsor category [1] 313805 0
Individual
Name [1] 313805 0
Chandra Parakash Rath
Address [1] 313805 0
Department of Neonatology
374 Bagot Road
Kind Edward Memorial Hospital
Subiaco WA-6008
Country [1] 313805 0
Australia

Ethics approval
Ethics application status
Submitted, not yet approved
Ethics committee name [1] 311596 0
Child and adoloscent health service human research ethics committee
Ethics committee address [1] 311596 0
Office 5E, Perth Children’s Hospital
15 Hospital Avenue, Nedlands WA 6009
Ethics committee country [1] 311596 0
Australia
Date submitted for ethics approval [1] 311596 0
29/09/2022
Approval date [1] 311596 0
Ethics approval number [1] 311596 0

Summary
Brief summary
Premature babies (born before 8 months of pregnancy) are at risk necrotising enterocolitis (NEC), a potentially serious inflammatory condition of the bowel, as well as hospital acquired infections, and poor nutrition. Complications of prematurity such as these, especially NEC, increase the risk of death, and long-term disability. The risk of these complication is high especially in extremely premature babies born before 28 weeks of pregnancy. Probiotics are beneficial bacteria which have been shown to significantly reduce the risk of death, NEC, and hospital acquired infections whilst facilitating nutrition in very premature babies. Probiotic supplementation for very premature babies is a standard practice in all neonatal intensive care units (NICU) in Australia, New Zealand and many units in other countries.
We currently administer a daily dose of 3 billion probiotic bacteria for premature babies in our unit using a product imported from Japan, under a special permission from the Australian government. This dose is based on our research using this product and studies of other probiotics. This study is designed to assess if a dose higher than 3 billion bacteria per day is more effective whilst being safe in reducing inflammation and improving the balance of beneficial versus potentially harmful bacteria in the gut of extremely premature babies.
Specifically, the proposed study will compare the dose of 3 billion against 6 and 9 billion bacteria per day in extremely premature babies using the stool (poo) samples. We think that babies who receive higher dose of probiotics will have reduced gut inflammation, more beneficial and less harmful bacteria in the gut and overall health compared to those who receive lower dose.
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 121658 0
Dr Chandra Prakash Rath
Address 121658 0
Department of Neonatology
King Edward Memorial Hospital for Women
374 Bagot road
Subiaco- 6008
WA
Country 121658 0
Australia
Phone 121658 0
+61452549299
Fax 121658 0
Email 121658 0
[email protected]
Contact person for public queries
Name 121659 0
Chandra Prakash Rath
Address 121659 0
Department of Neonatology
King Edward Memorial Hospital for Women
374 Bagot Road
Subiaco- 6008
WA
Country 121659 0
Australia
Phone 121659 0
+61 0864582222
Fax 121659 0
Email 121659 0
[email protected]
Contact person for scientific queries
Name 121660 0
Chandra Prakash Rath
Address 121660 0
Department of Neonatology
King Edward Memorial Hospital for Women
374 Bagot Road
Subiaco- 6008
WA
Country 121660 0
Australia
Phone 121660 0
+61 0864582222
Fax 121660 0
Email 121660 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
What data in particular will be shared?
De-identified individual data shall be available for sharing.
When will data be available (start and end dates)?
Immediately following publication to 15 years after that.(After approval of institutional ethics committee)
Available to whom?
Researchers who will provide a methodologically sound proposal.
Available for what types of analyses?
For approved proposals and IPD meta-analysis.
How or where can data be obtained?
By contacting the principal investigator ([email protected])


What supporting documents are/will be available?

Doc. No.TypeCitationLinkEmailOther DetailsAttachment
17141Study protocol    Attachment 384650-(Uploaded-27-09-2022-00-58-31)-Study-related document.docx
17142Informed consent form    Attachment 384650-(Uploaded-19-09-2022-15-11-21)-Study-related document.docx



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.