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临床试验/ACTRN12615001351505
ACTRN12615001351505已完成未知

A randomized double-blind placebo-controlled trial of gut microbiome transfer for the treatment of obesity in adolescents.

niversity of Auckland0 个研究点目标入组 87 人开始时间: 2015年12月14日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
87

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
14 Years 至 18 Years(—)
性别
All

入选标准

  • Recipient subjects (40 males and 40 females):
  • Age 14-18 years
  • Obese (BMI: greater or equal than 30 kg/m2)
  • Post-pubertal (Tanner stage 5)
  • Gut microbiome donors:
  • Age 18-28 years
  • BMI greater than 18.5 kg/m2 and less than 30.0 kg/m2
  • Total body fat percentage: less than or equal to 29% for females; less than or equal to 19% for males
  • Regular exercise (moderate to vigorous physical activity for at least 3.5 hours/week)
  • Regular Bowel Habit (at least 1 every 2 days)
  • Intake greater than or equal to 4 portions of fruit and/or vegetables per day

排除标准

  • Any transmissible viral or bacterial pathogens, or intestinal parasites
  • Multidrug-resistant organisms (e.g. vancomycin-resistant enterococci, extended-spectrum beta-lactamase-producing Enterobacteriaceae, and carbapenem-resistant Enterobacteriaceae)
  • Gastrointestinal disease (including symptoms of irritable bowel syndrome, inflammatory bowel disease, or coeliac disease)
  • Atopic diseases requiring regular prophylaxis or treatment
  • Current or past history of malignancy
  • Impaired fasting glucose or impaired glucose tolerance
  • Type 1 diabetes, type 2 diabetes, or monogenic diabetes
  • Known dyslipidaemia, hypertension, or metabolic syndrome
  • Regular use of medications known to influence metabolism or the gut microbiome
  • Use of oral antibiotics in the past three months
  • Regular 'binge drinking', i.e. consumption of 5 or more standard drinks of alcohol per session, at least once a week
  • Any use of recreational drugs or tobacco
  • Current or past pregnancy
  • Overseas travel in previous 6 months, except for visits to Australia, UK, USA, Canada, Northern Europe, France, and Germany.
  • UK residence in 1980–1996 (due to risk of variant Creutzfeldt-Jakob disease)
  • Recipients:
  • Gastrointestinal disease (including inflammatory bowel disease or coeliac disease)
  • Use of regular medications that may influence weight, metabolism, or the gut microbiome (including oral oestrogen-containing contraceptives, antidepressants, glucose-lowering drugs, diet drugs, as well as inhaled, topical, or oral steroids)
  • Consumption of probiotics
  • Type 1 diabetes, type 2 diabetes, or monogenic diabetes
  • Chronic diseases that could affect the primary outcome (other than obesity-related conditions)
  • Food allergies
  • Allergy to macrogol (active ingredient in the bowel preparation product)
  • Allergy to any over-the-counter medication
  • No antibiotic usage for three months prior to trial treatment

研究者

发起方
niversity of Auckland

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