Probiotic Supplementation During Pregnancy in Women With High-Risk Pregnancies
NCT ID: NCT06700044
Last Updated: 2024-12-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
150 participants
INTERVENTIONAL
2024-12-10
2027-12-31
Brief Summary
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Detailed Description
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GutMagnific is an evidence-based probiotic dietary supplement, shown to be effective in correcting disturbances in the gut microbiome, reduce inflammation and repair a damaged gut barrier. It was originally developed for treatment of irritable bowel syndrome (IBS). There is an overlap in immunological responses involved in PE and IBS, and women with IBS have a higher risk of developing PE. Therefore, the investigators expect that the product might also have positive effects in pregnant women with a high risk of PE.
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
QUADRUPLE
Study Groups
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High-risk probiotic
50 pregnant women with high risk of developing PE will take one stick/10\^9 CFU of probiotic dietary supplement GutMagnific per day from gestational week 12 until partus.
GutMagnific
Participants will take one stick/10\^9 CFU of probiotic dietary supplement GutMagnific per day from gestational week 12 until gestational week 37
High-risk placebo
50 pregnant women with high risk of developing PE will take one stick/placebo per day from gestational week 12 until partus.
Placebo
Participants will take one stick/placebo per day from gestational week 12 until partus.
Low-risk probiotic
25 pregnant women with low risk of developing PE will take one stick/10\^9 CFU of probiotic dietary supplement GutMagnific per day from gestational week 12 until partus.
GutMagnific
Participants will take one stick/10\^9 CFU of probiotic dietary supplement GutMagnific per day from gestational week 12 until gestational week 37
Low-risk placebo
25 pregnant women with low risk of developing PE will take one stick/placebo per day from gestational week 12 until partus.
Placebo
Participants will take one stick/placebo per day from gestational week 12 until partus.
Interventions
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GutMagnific
Participants will take one stick/10\^9 CFU of probiotic dietary supplement GutMagnific per day from gestational week 12 until gestational week 37
Placebo
Participants will take one stick/placebo per day from gestational week 12 until partus.
Eligibility Criteria
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Inclusion Criteria
* High risk of PE (≥ 1 high-risk factor, or ≥3 moderate risk factors according to the Swedish Society of Obstetrics and Gynecology (SFOG) 2019 guidelines); or low risk of PE (no high-risk factors, or \<3 moderate risk factors):
* High risk factors are:
* Auto-immune diseases such as SLE or anti-phospholipid syndrome
* Previous preeclampsia or eclampsia
* Previous hypertension of pregnancy with preterm birth before gestational week 34, growth restriction, intrauterine fetal death or ablatio
* Type 1 or 2 diabetes
* Duplex (or triplex) pregnancy
* Kidney disease
* Chronic hypertension
* IVF with egg donation
* Moderate risk factors are:
* Nulliparity
* Heredity for preeclampsia (at least one of mother, maternal grandmother, or sister)
* BMI\>30
* Age\>40
* Pregnancy interval \>10 years
* Systolic blood pressure \>130 mmHg or diastolic blood pressure \> 80 mmHg at admission in antenatal maternity care
* African descent
* Verified obstructive sleep apnea
* Ability to give written informed consent
Exclusion Criteria
* Use of other probiotic supplements in the last 2 weeks before baseline, or during the course of the study
* Use of antibiotics in the last 6 weeks
* Current treatment with metformin, progesterone, or regular medical treatment which may impact study aim (e.g. laxatives)
* Immunosuppression
* Diabetes mellitus (type I and type II)
* Inflammatory bowel disease
* Celiac disease
* Bad obstetric history
* Other serious conditions that might affect gut flora or capability of the subject to participate
* Language difficulties or difficulties understanding informed consent
18 Years
FEMALE
No
Sponsors
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ImmuneBiotech Medical Sweden AB
INDUSTRY
Region Skane
OTHER
Responsible Party
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Locations
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Region Skåne
Lund, , Sweden
Countries
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Central Contacts
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Facility Contacts
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Stefan Hansson
Role: primary
Other Identifiers
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Dnr 2024-03036-02
Identifier Type: -
Identifier Source: org_study_id