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WithdrawnNCT03858816Updated Mar 21, 2022

Efficacy of Multiple Strain Probiotics Reduces the Neurobehavioral Disorder in Premature Very Low Birth Weight Infants

An interventional study of Mixture probiotics and Placebo in Very Low Birth Weight Infants, sponsored by China Medical University Hospital. Withdrawn at 1 site in Taiwan. Per ClinicalTrials.gov, last updated 2022-03-21.

Sponsored by China Medical University Hospital · Not applicable, Interventional, and Treatment

Why this study was withdrawn
Difficulties in recruiting participants.

From the registry’s dates

  • Registered 8 months after the study started (first participant enrolled Jun 2018, registered Feb 2019).
Phase
Not applicable
Study type
Interventional
Enrollment
0
Allocation
Randomized
Sex
All
01

Study summary

The management protocols, clinical practices, equipment, infrastructure, and key personnel in NICU are unchanged during the study period. The data collected by each center are transmitted to the office of the principal investigator (Dr Lin) at China Medical University Hospital. Primary outcome is death or attention deficit and hyperactivity disorder (ADHD) and ASD.

Read the detailed description

Over the years, preterm very low birth weight (PVLBW) infants (\<32 weeks gestation) have better survival rates and improved outcomes. Nonetheless, It is of concern that there are increased risk of psychiatric problems reported in PVLBW infants, 11.5% to 31% of them are reported to be at increased risk of attention deficit and hyperactivity disorder (ADHD) and 25 % of them would develop autism spectrum disorder (ASD).

Many VLBWs experience rapid vaginal or Caesarean births that increased relative risk of developing ASD and possibly ADHD when compared to vaginal delivery. Further, PVLBW infants often experience delays in enteral feeding, and many receive little or no mother's own milk, use of antibiotics, invasive procedures and maternal separation can contribute to dysbiosis and dysbiosis in early life may prone to develop ASD and ADHD There is growing body of evidence demonstrates that gut microbiota is involved in communication, and may impact brain development and modulate behavior. Evidences have showed that there were increased intestinal permeability, altered gut microbiota and activity in autism and ADHD. Studies have demonstrated that early postnatal phase of microbial development is a primer for future health. Giving all the evidence, it is reasonable to speculate that probiotics could reduce the ASD and ADHD in preterm VLBW infants.

From Aug 1, 2017 to June 30, 2020, a prospective, double blind, randomized, controlled trial will be conducted in five NICUs at Taiwan. The study protocol will be approved by the institutional review board of each hospital. Preterm infants ≧ 23 weeks and ≦ 32 weeks gestational age and birth weight below 1500 gm and who survive to NICU are eligible for the trial. They will be assigned randomly to either group A: multiple strian probiotics or group B: control group received 1 mL of a 5% glucose solution. Study is continuous until preterm infants grow up to 4 months postnatal age.

The management protocols, clinical practices, equipment, infrastructure, and key personnel in NICU are unchanged during the study period. The data collected by each center are transmitted to the office of the principal investigator (Dr Lin) at China Medical University Hospital. Primary outcome is death or attention deficit and hyperactivity disorder (ADHD) and ASD.

Mortality is defined as death prior to discharge. Secondary outcomes are NEC ≧ stage 2, sepsis, severe (grade 3-4) IVH, BPD, alteration of liver function, and adverse effects or intolerance and neurodevelopment impairment. Objection of the first two years is to enroll cases, ASD and ADHD will be assessed by two independent neurologists at third year of life; no examiner is aware of treatment assigned to any infant.

02

Conditions studied

  • Very Low Birth Weight Infants

Keywords

  • probiotics
  • neuropsychiatric disorder
  • very low birth weight infants
  • attention deficit and hyperactivity disorder (ADHD)
  • autism spectrum disorder (ASD)
03

In context

Body Weight

1,223 studies on the registry are indexed under Body Weight; 131 are open to participants now.

Browse Body Weight studies →

Lead sponsor

China Medical University Hospital is the lead sponsor of 464 studies on the registry; 116 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Preterm infants ≧ 23 weeks and ≦ 32 weeks gestational age.
  • Birth weight below 1500 gm and who survive to NICU.

Exclusion criteria

Exclusion Criteria:

  • Severe asphyxia (stage III)
  • Fetal chromosomal anomalies
  • Cyanotic congenital heart disease
  • Congenital intestinal atresia
  • Gastroschisis
  • Omphalocele
  • Active upper gastric intestinal bleeding
  • Lacking/refused of parental consent
  • Early onset sepsis (before the third day of life)
  • Liver failure (aspartate aminotransferase, alanine aminotransferase, glutamyl transferase, direct bilirubin serum values 3-fold higher than reference range)
  • Fasted for >3 weeks.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    Mixture probiotics

    The probiotic contain 1 ×10\^9 CFU/1 capsule of mixture probiotics, taking 1 probiotic capsule for up to 4 months after birth.

    Other: Mixture probiotics

  • Placebo comparator
    Placebo

    Taking 1 placebo capsule for up to 4 months after birth.

    Other: Placebo

Interventions

  • OtherMixture probiotics

    The mixture probiotics capsule

  • OtherPlacebo

    The placebo contains the same excipient ingredients but without the live bacteria.

06

What researchers measure

Primary outcomes

  1. Incidence rate of death or ADHD and ASD

    Time frame: Two years

Secondary outcomes

  1. Incidence rate of NEC ≧ stage 2, sepsis, severe (grade 3-4) IVH, BPD, liver function and adverse effects or intolerance and neurodevelopment impairment.

    Time frame: Two years

07

Study locations

1 site
  • Department of Pediatrics, Children Hospital, China Medical University
    Taichung, 404, Taiwan
08

References and documents

Related links

Individual participant data

Plan to share: Yes — De-identified individual participant data for all primary and secondary outcome measures will be made available.

Supporting information: Study protocol, Sap, Icf, Csr, Analytic code

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 21, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03858816
Lead sponsor
China Medical University Hospital
Responsible party
Hung-Chih Lin (Attending physician, China Medical University Hospital) — Principal investigator
First posted
Mar 1, 2019
Start date
Jun 14, 2018
Primary completion
Jun 30, 2020 (estimated)
Completion
Jun 30, 2021 (estimated)
Last update
Mar 21, 2022

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Mar 2022. You cannot join it, but the record below documents what was studied.

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