跳至主要内容
临床试验/NCT02693041
NCT02693041已完成不适用

Pregnancy Complications - A Probiotic Interventional Study

Sahlgrenska University Hospital, Sweden1 个研究点 分布在 1 个国家目标入组 105 人开始时间: 2012年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
105
试验地点
1
主要终点
Inflammatory modulation of Lactobacillus Rhamnosus in low risk mothers.

研究概览

简要总结

Investigators hypothesize that

a) probiotics decrease the overall inflammatory state in the pregnant woman, especially in women with high risk pregnancies.

详细描述

The main of the Project is to determine if dietary supplementation intake of probiotics are associated with a decreased inflammatory response in pregnant women, especially those with a history of previous preterm birth or preeclampsia, in a randomized clinical trial. Investigators also want to further investigate the relationship between intake of probiotics and the degree of inflammation in different compartments during pregnancy to see how the probiotic components affect the inflammatory state in the women.

研究设计

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

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

  • Maternal age > or = 18 y
  • Singleton pregnancy
  • Nulli or multiparous without maternal intercurrent diseases or pregnant women with a history of spontaneous preterm delivery or pregnant women with a history of preeclampsia.
  • Exclusion Criteria
  • Multiple pregnancy
  • Gestational age > 17+6 weeks at first visit
  • Chronic intermittent diseases (e.g. diabetes mellitus, systemic lupus erythematosus, rheumatoid arthritis, Chron disease, ulcerative colitis)
  • Uterus malformations
  • Immunomodulatory medication
  • Hormonal treatment (e.g. crinone, progesterone)
  • Subject disagrees to stop intake of other products containing probiotics during study time.
  • Subject is unable to provide written informed consent

排除标准

  • 未提供

研究组 & 干预措施

PROBIOTIC in low-risk women

Active Comparator

In low-risk women, probiotic group will be treated with the Active ingredient containing Lactobacillus rhamnosus (LGG) (> 10x8 CFU) during all pregnancy until delivery. Capsules contain maltodextrin, LGG and vegetal magnesium stearate.

干预措施: probiotic (Drug)

PLACEBO in low-risk women

Placebo Comparator

In low-risk women, placebo group will be treated with the placebo ingredient during all pregnancy until delivery. The capsules of the placebo Group have similar content but lack the probiotic lactic acid bacteria which has been replaced by maltodextrin to make the mg amount equal.

干预措施: placebo (Drug)

PROBIOTIC in women with a prior PTB

Active Comparator

In women with a prior preterm birth (PTB), probiotic Group will be treated with the Active ingredient containing Lactobacillus rhamnosus (LGG) (> 10x8 CFU) during all pregnancy until delivery. Capsules contain maltodextrin, LGG and vegetal magnesium stearate.

干预措施: probiotic (Drug)

PLACEBO in women with a prior PTB

Placebo Comparator

In women with a prior preterm birth (PTB), placebo group will be treated with the placebo ingredient during all pregnancy until delivery. The capsules of the placebo Group have similar content but lack the probiotic lactic acid bacteria which has been replaced by maltodextrin to make the mg amount equal.

干预措施: placebo (Drug)

PROBIOTIC in women with a prior PE

Active Comparator

In women with a prior preeclampsia (PE), probiotic Group will be treated with the Active ingredient containing Lactobacillus rhamnosus (LGG) (> 10x8 CFU) during all pregnancy until delivery. Capsules contain maltodextrin, LGG and vegetal magnesium stearate.

干预措施: probiotic (Drug)

PLACEBO in women with a prior PE

Placebo Comparator

In women with a prior preeclampsia (PE), placebo Group will be treated with the placebo ingredient during all pregnancy until delivery. The capsules of the placebo Group have similar content but lack the probiotic lactic acid bacteria which has been replaced by maltodextrin to make the mg amount equal.

干预措施: placebo (Drug)

结局指标

主要结局

Inflammatory modulation of Lactobacillus Rhamnosus in low risk mothers.

时间窗: at recruitment, week 25, week 35 of gestation

Intake of LGG Rhamnosus throughout the pregnancy and its effect on levels of subpopulations of lymphocytes in peripheral blood (T/B/NK-celler), and cytokine production (TNF alfa, IL10, IL12) after stimulation with E. Coli, L. paracasei and P. aerugnousa, measuring change from baseline to 25 and 35 weeks gestation.

Inflammatory modulation of Lactobacillus Rhamnosus in mothers with previous preterm birth.

时间窗: at recruitment, week 25, week 35 of gestation

Intake of LGG Rhamnosus throughout the pregnancy and its effect on levels of subpopulations of lymphocytes in peripheral blood (T/B/NK-celler), and cytokine production (TNF alfa, IL10, IL12) after stimulation with E. Coli, L. paracasei and P. aerugnousa, measuring change from baseline to 25 and 35 weeks gestation.

Inflammatory modulation of Lactobacillus Rhamnosus in mothers with previous preeclampsia.

时间窗: at recruitment, week 25, week 35 of gestation

Intake of LGG Rhamnosus throughout the pregnancy and its effect on levels of subpopulations of lymphocytes in peripheral blood (T/B/NK-celler), and cytokine production (TNF alfa, IL10, IL12) after stimulation with E. Coli, L. paracasei and P. aerugnousa, measuring change from baseline to 25 and 35 weeks gestation.

次要结局

未报告次要终点

研究者

发起方
Sahlgrenska University Hospital, Sweden
申办方类型
Other
责任方
Principal Investigator
主要研究者

Bo Jacobsson

Clinical professor

Sahlgrenska University Hospital, Sweden

研究点 (1)

Loading locations...

相似试验