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临床试验/NCT05278130
NCT05278130撤回不适用

Serial Screening and Treatment of Bacterial Vaginosis in Pregnancy to Prevent Preterm Delivery: A Randomized Control Trial

Loma Linda University2 个研究点 分布在 1 个国家目标入组 600 人开始时间: 2022年10月20日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
入组人数
600
试验地点
2
主要终点
Number of participants with premature delivery (before 37 weeks gestation)

研究概览

简要总结

The purpose of this investigator-initiated randomized control trial is to determine if bacterial vaginosis infection increases the likelihood of preterm delivery in women with history of preterm delivery. Subjects will be randomized in a two-arm study to undergo predetermined intervals of testing for bacterial vaginosis or control.

详细描述

Preterm delivery affects 10% of all pregnancies in the United States. This risk is further increased in pregnant women with a history of preterm delivery. There are multiple etiology contributing of preterm labor. Of these, the presence of inflammation and infection have been a well-established cause. Bacterial vaginosis (BV), a common vaginal infection in pregnancy, may often be asymptomatic. Studies demonstrate a strong association between BV and preterm labor. Therefore it is recommended that women at high risk for preterm delivery are treated for this infection irregardless of symptoms. In this study the investigators hypothesize that increased testing for bacterial vaginosis, with subsequent timely treatment, may decrease the risk of preterm delivery in patients who are at high risk. The investigators suspect that the increase in monitoring will help diagnose asymptomatic bacterial vaginosis infections allowing for prompt treatment and avoidance of preterm labor.

Subjects will be randomized in a two-arm study to undergo predetermined intervals of testing for bacterial vaginosis or control. No experimental drugs or devices will be used.

  • The intervention-arm will have a pelvic exam performed with vaginal swab collection at their initial obstetric visit. The women undergoing the intervention will then subsequently undergo additional vaginal swab collections in 2 week intervals starting at 16 weeks gestational age until 34 weeks gestational age.
  • The control arm will undergo the standard of care. There will be no placebo for the control group.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

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

入选标准

  • Age greater than or equal to 18 years old
  • Pregnancy at less than 32 weeks gestational age at initial obstetric visit with Loma Linda Maternal Fetal Medicine (MFM) Clinic
  • History of at least one prior preterm delivery >16 and <37 weeks not due to iatrogenic indications, or short cervical length <2.5cm
  • Willing to receive prenatal standard of care and comply with treatment plan and other study procedures at Loma Linda

排除标准

  • Patients not deemed to be high risk for preterm delivery
  • Patient with cervical dilation ≥1cm on initial exam or with protruding membranes
  • Current pregnancy is multigestation
  • Medical indications for iatrogenic preterm delivery during this pregnancy (e.g. preeclampsia with severe features)
  • Desires termination during this pregnancy

结局指标

主要结局

Number of participants with premature delivery (before 37 weeks gestation)

时间窗: At delivery

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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