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临床试验/NCT00217308
NCT00217308撤回1 期

Effect of Probiotic Lactobacilli on Vaginal Flora of Pregnant Women at High Risk for Preterm Delivery

Mount Sinai Hospital, Canada1 个研究点 分布在 1 个国家开始时间: 2005年2月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
撤回
试验地点
1
主要终点
Determination if restoration of a normal vaginal flora through the use of probiotics reduces the incidence of PTB.

研究概览

简要总结

Purpose of the study is to determine the effect of probiotic lactobacilli on the vaginal flora and cytokine profile during pregnancy, and the incidence of preterm labour in women at high risk for preterm birth.

详细描述

Preterm labour involves multiple causes - one of the most significant factors being a prior history of preterm birth. Infection is another major cause of preterm labour (PTL) and is estimated to cause up to 30% of PTL. Bacterial Vaginosis (BV) is an alteration in the endogenous vaginal microflora preceded by a decreased presence of Lactobacilli species and increased growth of gardnerella and other pathogens. BV is a strong risk factor for PTL, and is associated with a 40% increased risk in some populations. Initial studies suggested that the treatment of BV with antibiotics could decrease the incidence of PTL, but this has not been confirmed by randomized trials. There is substantial evidence that the "normal" lactobacillus dominated urogenital microflora play an important role in maintenance of a healthy urinary and reproductive tract.

One hundred and sixty (160) women at high risk for PTL, based on a prior history of preterm birth, will be approached at their first antenatal visit to participate. Recruitment of 54 patients with symptomatic or asymptomatic BV (based on Nugent Scoring). Women with documented BV will be randomized to either treatment with lactobacilli preparation (n=27) or placebo (n=27). Women with symptomatic BV will be treated with oral Metronidazole prior to starting the lactobacilli or placebo. None of the subjects, researchers or clinical staff will know which preparation each woman receives.

This study will be the first to examine the ability of lactobacilli preparations to maintain a normal vaginal flora in pregnant women. In addition, the results will potentially serve as the basis for a multi-centre RCT to determine efficacy of this treatment in preventing preterm birth.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • pregnant women with previous incidence of preterm labour
  • otherwise healthy
  • over 18 years of age
  • able to provide informed consent
  • less than or equal to 16 weeks gestation
  • singleton pregnancy
  • normal uterine cavity

排除标准

  • significant medical complications (preeclampsia, thrombophilia, hypertension)
  • multiple pregnancy
  • less than 18 years of age
  • patients receiving antibiotics or other antimicrobial therapies at time of recruitment
  • fetal complications such as intrauterine growth restriction or other abnormalities
  • documented need for cervical cerclage
  • patient enrolled in other clinical trials

研究组 & 干预措施

Lactobacillus

Experimental

干预措施: Lactobacilli GR-1 and RC-14 (Drug)

Placebo capsules

Placebo Comparator

干预措施: Lactobacilli GR-1 and RC-14 (Drug)

结局指标

主要结局

Determination if restoration of a normal vaginal flora through the use of probiotics reduces the incidence of PTB.

时间窗: 12 weeks

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Alan Bocking

Clinician Scientist

Mount Sinai Hospital, Canada

研究点 (1)

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