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Effect of Probiotics (Vivomixx®) on Weight, Microbiota and Glucose Tolerance in Obese Pregnant Women and Their Newborn

The POP-study: Effect of Probiotics on Weight, Microbiota and Glucose Tolerance in Obese Pregnant Women and Their Newborn - a Randomized, Double-blind Placebo Controlled Trial With Vivomixx®

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02508844
Acronym
POP
Enrollment
50
Registered
2015-07-27
Start date
2015-04-30
Completion date
2020-03-31
Last updated
2020-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gestational Diabetes Mellitus, Obesity, Pregnancy

Keywords

Probiotics, Vivomixx®, Microbiota

Brief summary

The purpose of the study is to investigate if the probiotics Vivomixx® can affect gestational weight gain, microbiota and pregnancy complications in pregnant obese women and birth weight body composition of their infants.

Detailed description

Accumulating evidence indicates that the gut microbiota plays a significant role in obesity and because the ideal composition of the gut microbiota remains poorly understood, modulation of the gut microbiota composition represents a potentially attractive treatment option against excessive gestational weight gain and adverse outcomes for obese pregnant women and their newborn. Dietary supplements in the form of probiotics could be an efficient treatment for controlling weight gain in pregnancy by inducing changes in the gut microbiota and could have influence on infant's microbiota, which could have important implications for infant development and health. A pilot study including 50 obese pregnant nulliparous with BMI between 30-35 kg/m2 will, after accepting participation, be randomized to receive daily placebo or probiotics (four capsules of Vivomixx®; total of 450 billion CFU/day) from gestational age 14-20 until delivery. The infants will be followed until 9 months of age. Shortly after birth, tissue composition will be measured in the infants by DEXA-scanning. The women will be monitored by weight, blood-, fecal- and urine samples, diet questionnaires and hospital record review. Vivomixx® is a probiotic mixture of 8 probiotic strains, (Bifidobacterium breve, Bifidobacterium longum, Bifidobacterium infantis, Lactobacillus acidophilus, Lactobacillus plantarum, Lactobacillus paracasei, Lactobacillus bulgaricus and Streptococcus thermophilus). This is the first pilot study in which the probiotic Vivomixx® are added in a randomized fashion to the standard of care in obese pregnant women. 50 pregnant women are planned to be included. The aim of this group size is to clarify the feasibility, compliance and to estimate parameters such as the standard deviation which will be used in a sample size calculation for a full-scale trial.

Interventions

DIETARY_SUPPLEMENTVivomixx®

probiotics intake (four capsules of Vivomixx®; total of 450 billion CFU/day) from gestational age 14-20 until delivery

DIETARY_SUPPLEMENTPlacebo

Four capsules/day from gestational age 14-20 until delivery. The placebo capsule contains microcrytalline cellulose, magnesium stearate and silicon dioxide.

Sponsors

University of Copenhagen
CollaboratorOTHER
Statens Serum Institut
CollaboratorOTHER
Hvidovre University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* BMI ≥ 30 and ≤35 kg/m2- calculated from pre-pregnancy weight * Primiparous singleton pregnancy * Able to read and speak Danish * Normal ultrasound scan of the fetus at gestational age 12-14 * Oral glucose tolerance test at gestational age 14-20

Exclusion criteria

* Pregnancy at \> 20 weeks gestation at recruitment * Pre-gestational diabetes or other serious diseases * Multiple pregnancy * Previous bariatric surgery * Ingestion of probiotics \< 1 month before the inclusion or ingestion of other kinds of probiotics than the study probiotics

Design outcomes

Primary

MeasureTime frameDescription
Gestational weight gainweek 36-37 of pregnancyweight at gestational age 36-37-weeks minus self-reported pre-pregnancy weight
Change in glucose levels (Oral glucose tolerance test)baseline (week 14-20) and 27-30 of pregnancy

Secondary

MeasureTime frameDescription
Change in fecal microbiotabaseline (week 14-20) and week 36-37 of pregnancy
Amount of fat tissue in the newborn infantat birthexamined by a DEXA-scanning
Change in HbA1cbaseline (week 14-20) and week 36-37 of pregnancy

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026