Synbiotics in Patients at RIsk fOr Preterm Birth (PRIORI)
Preterm Spontaneous Labor With Preterm Delivery, Preterm Birth, Microbial Colonization
About this trial
This is an interventional other trial for Preterm Spontaneous Labor With Preterm Delivery focused on measuring Preterm birth, Vaginal microbiome, Probiotics, Synbiotics
Eligibility Criteria
Inclusion Criteria: Signed written informed consent must be obtained before any study assessment is performed; 18 years of age or older; Singleton pregnancy; Pregnancy consultation between 8 and 10 weeks gestation. At least one of the following risk factors for spontaneous preterm birth: Prior spontaneous preterm birth, defined as delivery between 24 and 37 weeks following PPROM, preterm labor or cervical insufficiency PPROM ≤37 weeks in previous pregnancy but delivery ≥37 weeks Prior spontaneous second-trimester pregnancy loss, defined as PPROM, preterm labor or cervical insufficiency with birth between 14 and 24 weeks. Exclusion Criteria: Patients who are already using pro-, pre- or synbiotics Multiple pregnancy Need for primary (type 1) cerclage Inflammatory bowel disease Known congenital uterine anomaly History of LLETZ conization
Sites / Locations
- Ziekenhuis Oost-LimburgRecruiting
- Universitaire Ziekenhuizen Leuven
- UZ GentRecruiting
- AZ Sint-JanRecruiting
- AZ Sint-LucasRecruiting
- CHR CitadelleRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Synbiotics
Placebo
Oral synbiotic (food supplement) containing 8 probiotic Lactobacillus strains, the prebiotics inulin, fructooligosaccharides (FOS) and D-mannose.
Matching placebo