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

Primary Purpose

Pregnancy, Obesity, Gestational Diabetes Mellitus

Status
Completed
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Vivomixx®
Placebo
Sponsored by
Hvidovre University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Pregnancy focused on measuring Probiotics, Vivomixx®, Microbiota

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

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

Sites / Locations

  • Hvidovre University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Vivomixx®

Placebo

Arm Description

Bifidobacterium breve, Bifidobacterium longum, Bifidobacterium infantis, Lactobacillus acidophilus, Lactobacillus plantarum, Lactobacillus paracasei, Lactobacillus bulgaricus and Streptococcus thermophilus

microcrytalline cellulose, magnesium stearate and silicon dioxide.

Outcomes

Primary Outcome Measures

Gestational weight gain
weight at gestational age 36-37-weeks minus self-reported pre-pregnancy weight
Change in glucose levels (Oral glucose tolerance test)

Secondary Outcome Measures

Change in fecal microbiota
Amount of fat tissue in the newborn infant
examined by a DEXA-scanning
Change in HbA1c

Full Information

First Posted
May 11, 2015
Last Updated
March 20, 2020
Sponsor
Hvidovre University Hospital
Collaborators
University of Copenhagen, Statens Serum Institut
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1. Study Identification

Unique Protocol Identification Number
NCT02508844
Brief Title
Effect of Probiotics (Vivomixx®) on Weight, Microbiota and Glucose Tolerance in Obese Pregnant Women and Their Newborn
Acronym
POP
Official Title
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®
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
April 2015 (undefined)
Primary Completion Date
January 2018 (Actual)
Study Completion Date
March 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hvidovre University Hospital
Collaborators
University of Copenhagen, Statens Serum Institut

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pregnancy, Obesity, Gestational Diabetes Mellitus
Keywords
Probiotics, Vivomixx®, Microbiota

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Vivomixx®
Arm Type
Experimental
Arm Description
Bifidobacterium breve, Bifidobacterium longum, Bifidobacterium infantis, Lactobacillus acidophilus, Lactobacillus plantarum, Lactobacillus paracasei, Lactobacillus bulgaricus and Streptococcus thermophilus
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
microcrytalline cellulose, magnesium stearate and silicon dioxide.
Intervention Type
Dietary Supplement
Intervention Name(s)
Vivomixx®
Intervention Description
probiotics intake (four capsules of Vivomixx®; total of 450 billion CFU/day) from gestational age 14-20 until delivery
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Four capsules/day from gestational age 14-20 until delivery. The placebo capsule contains microcrytalline cellulose, magnesium stearate and silicon dioxide.
Primary Outcome Measure Information:
Title
Gestational weight gain
Description
weight at gestational age 36-37-weeks minus self-reported pre-pregnancy weight
Time Frame
week 36-37 of pregnancy
Title
Change in glucose levels (Oral glucose tolerance test)
Time Frame
baseline (week 14-20) and 27-30 of pregnancy
Secondary Outcome Measure Information:
Title
Change in fecal microbiota
Time Frame
baseline (week 14-20) and week 36-37 of pregnancy
Title
Amount of fat tissue in the newborn infant
Description
examined by a DEXA-scanning
Time Frame
at birth
Title
Change in HbA1c
Time Frame
baseline (week 14-20) and week 36-37 of pregnancy

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andreas M Petersen, MD, PhD
Organizational Affiliation
Hvidovre University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hvidovre University Hospital
City
Hvidovre
State/Province
Copenhagen
ZIP/Postal Code
2650
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
32617453
Citation
Halkjaer SI, de Knegt VE, Lo B, Nilas L, Cortes D, Pedersen AE, Mirsepasi-Lauridsen HC, Andersen LO, Nielsen HV, Stensvold CR, Johannesen TB, Kallemose T, Krogfelt KA, Petersen AM. Multistrain Probiotic Increases the Gut Microbiota Diversity in Obese Pregnant Women: Results from a Randomized, Double-Blind Placebo-Controlled Study. Curr Dev Nutr. 2020 May 27;4(7):nzaa095. doi: 10.1093/cdn/nzaa095. eCollection 2020 Jul.
Results Reference
derived
PubMed Identifier
27724923
Citation
Halkjaer SI, Nilas L, Carlsen EM, Cortes D, Halldorsson TI, Olsen SF, Pedersen AE, Krogfelt KA, Petersen AM. Effects of probiotics (Vivomixx(R)) in obese pregnant women and their newborn: study protocol for a randomized controlled trial. Trials. 2016 Oct 11;17(1):491. doi: 10.1186/s13063-016-1617-5.
Results Reference
derived

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

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