Other Clinical Trial - Impact of Oral Probiotic Blend on Pregnancy Outcome

Status Completed

Clinical Trial Summary

The aim of this study is, to investigate the effect of oral intake of Lactobacillus rhamnosus GG (ATCC 53103), Lactobacillus crispatus Lbv88, Lactobacillus rhamnosus Lbv96, Lactobacillus jensenii Lbv116 Lactobacillus gasseri Lbv150 on outcomes of pregnancy and microbiota and their interrelation.

Clinical Trial Description

Pregnant women aged > 18 years in the < 14th week of pregnancy willing to consume the study product once daily starting the day after V1 until delivery, complying with inclusion and exclusion criteria will be enrolled in the study. After enrollement subjects will be randomly and evenly assigned to one of the two test groups verum and placebo. The study population will be recruited in a screening examination ( G1 ) by gynaecologists from Kiel area. Primary target parameter of the study : HOMA-IRa value in week 24-28 (V2), which is based on glucose and insulin measures during the second oral glucose tolerance test (OGTT) Secondary target parameters : HOMA-IR value in week 36-40 , Alteration (V2 - V1) Δ HOMA-IR, Alteration (V2 - V1) Δ QUICKI ;

Study Design

Related Conditions & MeSH terms

Diabetes, Gestational
Gestational Diabetes Mellitus in Pregnancy
Pregnancy in Diabetics

Clinical Trial Details

NCT number	NCT04009889
Study type	Interventional
Source	i-Health, Inc.
Contact
Status	Completed
Phase	N/A
Start date	April 5, 2018
Completion date	June 12, 2020

View Details

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