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Gestational Obesity and Interventions With Probiotics or Fish Oil Trial (GOPROFIT)

Primary Purpose

Obesity, Pregnancy, Inflammation

Status
Unknown status
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Fish Oil
Probiotic
Placebo
Sponsored by
Universidade Federal do Rio de Janeiro
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Obesity focused on measuring obesity, placenta, inflammation, fish oil, probiotics

Eligibility Criteria

19 Years - 40 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • aged between 19 and 40 years
  • gestational age of 13 weeks;
  • BMI prepregnancy greater than 29.9 and less than 40 kg / m² [ degrees obesity 1 and 2, according to the World Health Organization (WHO, 2002) ] or prepregnancy BMI between 18.5 and 24 9 kg / m² [ eutrophic ( WHO, 2002 ) ]
  • be free of chronic diseases (hypertension , cardiovascular disease, type 2 diabetes , thyroid diseases , cirrhosis , chronic hepatitis and chronic renal failure
  • be free of infectious and parasitic diseases
  • present gestation single fetus
  • not being a smoker
  • do not consume alcoholic beverages
  • do not consume supplement containing AG

Exclusion Criteria:

  • receive confirmation of diagnosis of chronic noncommunicable diseases (except obesity) and / or infectious
  • pregnant women who did not complete all the steps provided for in the study

Sites / Locations

  • Maternidade Escola da Universidade Federal do Rio de JaneiroRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Placebo Comparator

Experimental

Experimental

Experimental

Arm Label

Eutrophy Control

Eutrophy+ Probiotic

Obesity + Fish oil

Obesity + Probiotic

Arm Description

Gelatin capsules a day, from 28ª week to 36ª week gestation.

Capsules gastro resistant containing 2.5 billions colony forming unit (UFC) Lactobacillus rhamnosus GG + 2.5 billions colony forming unit (UFC) Bifidobacterium bifidum a day, from 28ª week to 36ª week gestation

DHA (100 mg) + EPA (137 mg) a day, from 13ª week gestation to 36ª week gestation

2.5 billions colony forming unit (UFC) Lactobacillus rhamnosus GG + 2.5 billions colony forming unit (UFC) Bifidobacterium bifidum a day, from 28ª week to 36ª week gestation

Outcomes

Primary Outcome Measures

Association between maternal obesity and systemic Inflammation in the Mother and the Activation of Placental Inflammatory Pathways
Association between fish oil intake in obese mothers and systemic Inflammation in the Mother and the Activation of Placental Inflammatory Pathways
Investigation of the effects of fish oil supplementation on the metabolome of maternal serum, umbilical cord serum and placenta in obese pregnant women.
The metabolome of maternal serum, umbilical cord serum and placenta of obese and healthy pregnant women was analyzed by nuclear magnetic resonance.
Association between probiotic supplementation and bacterial colonization in the maternal intestinal and vaginal microbiota
Evaluation of the maternal intestinal and vaginal microbiota through the quantification of bacteria

Secondary Outcome Measures

Association between maternal obesity and placental fatty acid transporter expression
Association between fish oil intake in obese mothers and placental fatty acid transporter
Association between maternal inflammatory status and pregnancy outcomes

Full Information

First Posted
July 10, 2017
Last Updated
July 10, 2017
Sponsor
Universidade Federal do Rio de Janeiro
Collaborators
Maternidade Escola da UFRJ
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1. Study Identification

Unique Protocol Identification Number
NCT03215784
Brief Title
Gestational Obesity and Interventions With Probiotics or Fish Oil Trial
Acronym
GOPROFIT
Official Title
Impact of Fish Oil or Probiotic Intake on Maternal Obesity and Molecular Biomarkers in the Placenta
Study Type
Interventional

2. Study Status

Record Verification Date
July 2017
Overall Recruitment Status
Unknown status
Study Start Date
March 2015 (undefined)
Primary Completion Date
September 2017 (Anticipated)
Study Completion Date
December 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidade Federal do Rio de Janeiro
Collaborators
Maternidade Escola da UFRJ

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Obesity is one of the most concerning health issues in the modern world, especially due to its association with greater risk of developing a wide range of chronic diseases. Pre-gestational obesity may increase the chances of maternal and fetal morbimortality, such as gestational diabetes mellitus, preeclampsia, macrosomia and, even, fetal death. It may also lead to long term disorders, enhancing the risk of excessive adiposity and metabolic syndrome in later life and, thus, contributing to the maintenance of the obesity cycle and its health effects through the subsequent generations. Alterations in placental function are thought to be deeply involved in this scenario, however further research on its molecular and biological mechanisms is needed. During pregnancy, there is a physiological enhancement of the inflammatory state, marked by higher circulating cytokines and macrophage placental infiltration, which favors fetal nutrient supply and adequate growth; however, this response is exacerbated in women with pre-pregnancy obesity, leading to adverse outcomes. In this context, interventions aiming to reduce excessive inflammation may prevent or minimize the negative impact of pre-pregnancy obesity on both maternal and offspring's health. There is strong evidence suggesting an important role of n-3 LC-PUFA (EPA and DHA) on the attenuation and resolution of inflammatory states, besides influencing maternal lipid profile, fetal and infant adipogenesis and neurodevelopment. Additionally, the consumption of probiotic supplements during gestation seams to promote adequate maternal weight gain and improve the profile of inflammatory molecules secreted in the milk. Therefore, the nutritional interventions with fish oil, as a source of EPA and DHA, or probiotics, in women with pre-pregnancy obesity, may change the intrauterine environment and reduce the risk of both short and long term metabolic disorders. This study aims to investigate the metabolic and molecular changes promoted by gestational obesity and evaluate the effectiveness of different dietary interventions (fish oil or probiotic) on preventing or minimizing such alterations. We expect to contribute to the understanding of the physiological and molecular mechanisms underlying maternal obesity and its association with adverse pregnancy outcomes, associated with increased risk of chronic diseases in adulthood.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Pregnancy, Inflammation
Keywords
obesity, placenta, inflammation, fish oil, probiotics

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Eutrophy Control
Arm Type
Placebo Comparator
Arm Description
Gelatin capsules a day, from 28ª week to 36ª week gestation.
Arm Title
Eutrophy+ Probiotic
Arm Type
Experimental
Arm Description
Capsules gastro resistant containing 2.5 billions colony forming unit (UFC) Lactobacillus rhamnosus GG + 2.5 billions colony forming unit (UFC) Bifidobacterium bifidum a day, from 28ª week to 36ª week gestation
Arm Title
Obesity + Fish oil
Arm Type
Experimental
Arm Description
DHA (100 mg) + EPA (137 mg) a day, from 13ª week gestation to 36ª week gestation
Arm Title
Obesity + Probiotic
Arm Type
Experimental
Arm Description
2.5 billions colony forming unit (UFC) Lactobacillus rhamnosus GG + 2.5 billions colony forming unit (UFC) Bifidobacterium bifidum a day, from 28ª week to 36ª week gestation
Intervention Type
Dietary Supplement
Intervention Name(s)
Fish Oil
Intervention Type
Dietary Supplement
Intervention Name(s)
Probiotic
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
Association between maternal obesity and systemic Inflammation in the Mother and the Activation of Placental Inflammatory Pathways
Time Frame
28 weeks
Title
Association between fish oil intake in obese mothers and systemic Inflammation in the Mother and the Activation of Placental Inflammatory Pathways
Time Frame
28 weeks
Title
Investigation of the effects of fish oil supplementation on the metabolome of maternal serum, umbilical cord serum and placenta in obese pregnant women.
Description
The metabolome of maternal serum, umbilical cord serum and placenta of obese and healthy pregnant women was analyzed by nuclear magnetic resonance.
Time Frame
28 weeks
Title
Association between probiotic supplementation and bacterial colonization in the maternal intestinal and vaginal microbiota
Description
Evaluation of the maternal intestinal and vaginal microbiota through the quantification of bacteria
Time Frame
36 weeks
Secondary Outcome Measure Information:
Title
Association between maternal obesity and placental fatty acid transporter expression
Time Frame
28 weeks
Title
Association between fish oil intake in obese mothers and placental fatty acid transporter
Time Frame
28 weeks
Title
Association between maternal inflammatory status and pregnancy outcomes
Time Frame
28 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: aged between 19 and 40 years gestational age of 13 weeks; BMI prepregnancy greater than 29.9 and less than 40 kg / m² [ degrees obesity 1 and 2, according to the World Health Organization (WHO, 2002) ] or prepregnancy BMI between 18.5 and 24 9 kg / m² [ eutrophic ( WHO, 2002 ) ] be free of chronic diseases (hypertension , cardiovascular disease, type 2 diabetes , thyroid diseases , cirrhosis , chronic hepatitis and chronic renal failure be free of infectious and parasitic diseases present gestation single fetus not being a smoker do not consume alcoholic beverages do not consume supplement containing AG Exclusion Criteria: receive confirmation of diagnosis of chronic noncommunicable diseases (except obesity) and / or infectious pregnant women who did not complete all the steps provided for in the study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Fátima Lúcia C Sardinha, PhD
Phone
(55) 21 996355046
Email
sardinhaflc@nutricao.ufrj.br
First Name & Middle Initial & Last Name or Official Title & Degree
Tatiana P El-Bacha, PhD
Phone
(55) 21 997667997
Email
tatiana@nutricao.ufrj.br
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fátima Lúcia C Sardinha, PhD
Organizational Affiliation
Instituto de Nutrição Josué de Castro/ UFRJ
Official's Role
Study Director
Facility Information:
Facility Name
Maternidade Escola da Universidade Federal do Rio de Janeiro
City
Rio de Janeiro
State/Province
RJ
ZIP/Postal Code
22240-000
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lívia B Almeida, Ms
Phone
(55) 21 991689325
Email
livia.belcastro@gmail.com
First Name & Middle Initial & Last Name & Degree
Daniela B Mucci, Ms
Phone
(55) 21 991960867
Email
danimucci@gmail.com
First Name & Middle Initial & Last Name & Degree
Danielle N Melo, Esp.
First Name & Middle Initial & Last Name & Degree
Camila M G Cortat, Ms

12. IPD Sharing Statement

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Gestational Obesity and Interventions With Probiotics or Fish Oil Trial

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