Article (Scientific journals)
Synbiotics in patients at risk for spontaneous preterm birth: protocol for a multi-centre, double-blind, randomised placebo-controlled trial (PRIORI).
Nulens, Katrien; Papy, Els; Tartaglia, Katrien et al.
2024In Trials, 25 (1), p. 615
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Keywords :
Lactobacilli; Next-generation sequencing; PPROM; Pregnancy; Prematurity; Preterm birth; Probiotics; Randomised controlled trial; Synbiotics; Vaginal microbiome; Humans; Female; Double-Blind Method; Risk Factors; Microbiota; Gestational Age; Infant, Newborn; Treatment Outcome; Vaginosis, Bacterial/microbiology; Vaginosis, Bacterial/diagnosis; Premature Birth/prevention & control; Synbiotics/administration & dosage; Multicenter Studies as Topic; Randomized Controlled Trials as Topic; Vagina/microbiology; Premature Birth; Vagina; Vaginosis, Bacterial; Medicine (miscellaneous); Pharmacology (medical)
Abstract :
[en] [en] BACKGROUND: Prematurity remains one of the main causes of neonatal morbidity and mortality. Approximately two thirds of preterm births are spontaneous, i.e. secondary to preterm labour, preterm prelabour rupture of membranes (PPROM) or cervical insufficiency. Etiologically, the vaginal microbiome plays an important role in spontaneous preterm birth (sPTB). Vaginal dysbiosis and bacterial vaginosis are well-known risk factors for ascending lower genital tract infections and sPTB, while a Lactobacillus crispatus-dominated vaginal microbiome is associated with term deliveries. Synbiotics may help to achieve and/or maintain a normal, Lactobacillus-dominated vaginal microbiome. METHODS: We will perform a multi-centre, double-blind, randomised, placebo-controlled trial. Women aged 18 years or older with a singleton pregnancy are eligible for inclusion at 80/7-106/7 weeks gestational age if they have one or more of the following risk factors for sPTB: previous sPTB at 240/7-356/7 weeks, prior PPROM before 360/7 weeks, or spontaneous pregnancy loss at 140/7-236/7 weeks of gestation. Exclusion criteria are multiple gestation, cervix conisation, inflammatory bowel disease, uterine anomaly, and the use of pro-/pre-/synbiotics. Patients will be randomised to oral synbiotics or placebo, starting before 11 weeks of gestation until delivery. The oral synbiotic consists of eight Lactobacillus species (including L. crispatus) and prebiotics. The primary outcome is the gestational age at delivery. Vaginal microbiome analysis once per trimester (at approximately 9, 20, and 30 weeks) and delivery will be performed using metataxonomic sequencing (16S rRNA gene) and microbial culture. Secondary outcomes include PPROM, the use of antibiotics, antenatal admission information, and neonatal outcomes. DISCUSSION: This study will evaluate the effect of oral synbiotics on the vaginal microbiome during pregnancy in a high-risk population and correlate the microbial changes with the gestational age at delivery and relevant pregnancy outcomes. TRIAL REGISTRATION: ClinicalTrials.gov, NCT05966649. Registered on April 5, 2024.
Disciplines :
Reproductive medicine (gynecology, andrology, obstetrics)
Author, co-author :
Nulens, Katrien ;  Department of Obstetrics and Gynaecology, Ziekenhuis Oost-Limburg, Genk, Belgium. katrien_nulens@hotmail.com ; Department of Development and Regeneration, KULeuven, Cluster Woman and Child, Leuven, Belgium. katrien_nulens@hotmail.com
Papy, Els;  Department of Obstetrics and Gynaecology, Ziekenhuis Oost-Limburg, Genk, Belgium
Tartaglia, Katrien;  Clinical Trial Unit, Ziekenhuis Oost-Limburg, Genk, Belgium
Dehaene, Isabelle;  Department of Obstetrics and Gynaecology, Ghent University Hospital, Ghent, Belgium
Logghe, Hilde;  Department of Obstetrics and Gynaecology, AZ Sint-Lucas, Bruges, Belgium ; Department of Obstetrics and Gynaecology, AZ Sint-Jan, Bruges, Belgium
Van Keirsbilck, Joachim;  Department of Obstetrics and Gynaecology, AZ Sint-Jan, Bruges, Belgium
Chantraine, Frédéric  ;  Université de Liège - ULiège > Département des sciences cliniques
Masson, Véronique ;  Université de Liège - ULiège > Département des sciences cliniques
Simoens, Eva;  Department of Obstetrics and Gynaecology, AZ Groeninge, Kortrijk, Belgium
Gysemans, Willem;  Department of Paediatrics and Neonatal Intensive Care Unit, Ziekenhuis Oost-Limburg, Genk, Belgium
Bruckers, Liesbeth;  Data Science Institute, I-Biostat, Hasselt University, Diepenbeek, Belgium
Lebeer, Sarah;  Department of Bioscience Engineering, Research Group Applied Microbiology and Biotechnology, University of Antwerp, Antwerp, Belgium
Allonsius, Camille Nina;  Department of Bioscience Engineering, Research Group Applied Microbiology and Biotechnology, University of Antwerp, Antwerp, Belgium
Oerlemans, Eline;  Department of Bioscience Engineering, Research Group Applied Microbiology and Biotechnology, University of Antwerp, Antwerp, Belgium
Steensels, Deborah;  Department of Microbiology, Ziekenhuis Oost-Limburg, Genk, Belgium ; Faculty of Medicine, Université Libre de Bruxelles, Brussels, Belgium
Reynders, Marijke;  Department of Microbiology, AZ Sint-Jan, Bruges, Belgium
Timmerman, Dirk;  Department of Development and Regeneration, KULeuven, Cluster Woman and Child, Leuven, Belgium ; Department of Obstetrics and Gynaecology, University Hospitals Leuven, Leuven, Belgium
Devlieger, Roland;  Department of Development and Regeneration, KULeuven, Cluster Woman and Child, Leuven, Belgium ; Department of Obstetrics and Gynaecology, University Hospitals Leuven, Leuven, Belgium
Van Holsbeke, Caroline;  Department of Obstetrics and Gynaecology, Ziekenhuis Oost-Limburg, Genk, Belgium ; Department of Obstetrics and Gynaecology, AZ Sint-Lucas, Bruges, Belgium ; Department of Obstetrics and Gynaecology, AZ Sint-Jan, Bruges, Belgium
More authors (9 more) Less
Language :
English
Title :
Synbiotics in patients at risk for spontaneous preterm birth: protocol for a multi-centre, double-blind, randomised placebo-controlled trial (PRIORI).
Publication date :
17 September 2024
Journal title :
Trials
eISSN :
1745-6215
Publisher :
BioMed Central Ltd, England
Volume :
25
Issue :
1
Pages :
615
Peer reviewed :
Peer Reviewed verified by ORBi
Funding text :
This study (KCE20-1273) is funded by the Belgian Health Care Knowledge Centre (KCE) under the KCE Trials Programme.
Available on ORBi :
since 15 May 2025

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