Clinical Trial

Probiotic Supplementation During Pregnancy in Women With High-Risk Pregnancies

Recruiting
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Summary
Preeclampsia (PE) is a complication during pregnancy characterized by hypertension, organ damage, and inflammation, without an effective treatment. The underlying mechanisms causing the disease also remain partly unknown. In this double-blind placebo-controlled study, the effects of probiotic dietary supplement GutMagnific during pregnancy will be assessed in pregnancies with a high risk of PE as well as low risk. The hypothesis is that probiotic dietary supplement GutMagnific can prevent or reduce the inflammatory response and clinical manifestations associated with PE through counteracting imbalances in the oral and gut microbiome composition.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2024-11-18.
Status change: Not Yet Recruiting → Recruiting 2024-12-20
Trial Details
NCT Number NCT06700044
Lead Sponsor Region Skane
Collaborators: ImmuneBiotech Medical Sweden AB
Conditions Preeclampsia, Gut Dysbiosis
Enrollment 150 participants
Start Date 2024-12-10
Primary Completion 2027-12 (estimated)
Study Completion 2027-12 (estimated)
Updated on ClinicalTrials.gov 2024-12-27