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临床试验/NL-OMON43160
NL-OMON43160已完成3 期

A randomized, double-blind, placebo-controlled, pilot trial of probiotics in pregnant women with symptoms of anxiety and depression. - PIP (Probiotics In Pregnancy)

Radboud Universiteit Nijmegen0 个研究点目标入组 40 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • 1. Healthy pregnant women in obstetric care in the Netherlands with at least elevated symptoms of depression and/or anxiety (resp. EDS * 10; STAI-S > 40)
  • 2. Women who can start daily probiotic intake from *26 weeks gestational age until delivery (Note: the upper limit of *26 weeks allows time to complete at least 8 weeks of probiotic intake prior to delivery) (Gestation is based on last menstrual period and early ultrasound).

排除标准

  • 1) Multiple pregnancy (increased obstetric risk);
  • 2) High suicidal risk according to suicidality subscale score on the MINI International Neuropsychiatric Interview;
  • 3) Illegal drug use;
  • 4) Having a psychiatric history on psychoses and bipolar disorder;
  • 5) Medically diagnosed with inflammatory bowel disease;
  • 6) History of major gastro-intestinal surgery (e.g. colectomy);
  • 7) Hypersensitivity or allergy to any ingredients in the probiotic product;
  • 8) History of using oral multi-species probiotic EcologicBarrier;
  • 9) Presently using food containing probiotics (Actimel etc.) and not willing to stop these at least 2 weeks prior to the start of the study;
  • 10) No mastery of the Dutch language.

研究者

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