对有自发性早产风险的患者使用合成益生菌:多中心、双盲、随机安慰剂对照试验(PRIORI)方案

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2024-09-17 DOI:10.1186/s13063-024-08444-8
Katrien Nulens, Els Papy, Katrien Tartaglia, Isabelle Dehaene, Hilde Logghe, Joachim Van Keirsbilck, Frédéric Chantraine, Veronique Masson, Eva Simoens, Willem Gysemans, Liesbeth Bruckers, Sarah Lebeer, Camille Nina Allonsius, Eline Oerlemans, Deborah Steensels, Marijke Reynders, Dirk Timmerman, Roland Devlieger, Caroline Van Holsbeke
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引用次数: 0

摘要

早产仍然是新生儿发病和死亡的主要原因之一。大约三分之二的早产是自然分娩,即继发于早产、早产胎膜早破(PPROM)或宫颈机能不全。从病因上讲,阴道微生物群在自发性早产(sPTB)中扮演着重要角色。众所周知,阴道菌群失调和细菌性阴道病是导致下生殖道感染和早产的风险因素,而以脆片乳杆菌为主的阴道微生物群则与足月分娩有关。合成益生菌可能有助于实现和/或维持正常的、以乳酸杆菌为主的阴道微生物群。我们将进行一项多中心、双盲、随机、安慰剂对照试验。年龄在 18 岁或 18 岁以上的单胎妊娠女性,如果具有以下一种或多种导致 sPTB 的风险因素,则有资格在孕龄 80/7-106/7 周时加入该试验:曾在孕龄 240/7-356/7 周时患过 sPTB、曾在孕龄 360/7 周前发生过 PPROM 或在孕龄 140/7-236/7 周时自然流产。排除标准包括多胎妊娠、宫颈锥切、炎症性肠病、子宫畸形,以及使用前/后/合生素。患者将被随机分配口服合生元或安慰剂,从妊娠 11 周前开始直至分娩。口服益生菌由八种乳酸杆菌(包括L. crispatus)和益生元组成。主要结果是分娩时的胎龄。将使用元分类测序(16S rRNA 基因)和微生物培养法对每个孕期(约 9 周、20 周和 30 周)和分娩进行一次阴道微生物组分析。次要结果包括 PPROM、抗生素的使用、产前入院信息和新生儿预后。本研究将评估口服合生元对高危人群孕期阴道微生物群的影响,并将微生物变化与分娩时的胎龄和相关妊娠结局联系起来。ClinicalTrials.gov,NCT05966649。注册日期:2024 年 4 月 5 日。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synbiotics in patients at risk for spontaneous preterm birth: protocol for a multi-centre, double-blind, randomised placebo-controlled trial (PRIORI)
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. 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. 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. ClinicalTrials.gov, NCT05966649. Registered on April 5, 2024.
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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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