JPRN-jRCTs031210451招募中未知
SYNbiotics Effect Research after sleeve Gastrectomy In Severely obese patients on intestinal flora: a double blind, randoMized controlled trial - SYNERGISM study
Kusumoto Tetsuya0 个研究点目标入组 30 人开始时间: 2021年11月26日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 30
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
- >= 20age old 至 <= 65age old(—)
- 性别
- All
入选标准
- •Patients who meet all of the following criteria are included in this study:
- •1. patients with severe obesity (whose BMI is 35 kg/m2 or more at the first visit)
- •2. patients with obesity-related complication (type 2 diabetes mellitus, hypertension, dyslipidemia, or sleep apnea syndrome)
- •3. patients who are planned to take laparoscopic sleeve gastrectomy due to the severe obesity in the medical institutions that conduct this study
- •4. patients who are aged of 20 years or older and 65 years or younger at giving their consent
- •5. patients who provide their consent in a written form by themselves after full explanation of this study
排除标准
- •Patients who fall into any of the following criteria are excluded from participating in the study:
- •1. patients with history of allergy against bifidobacteria, lactic acid bacteria, or galacto-oligosaccharide
- •2. patients who take supplements including prebiotics and probiotics other than the study food in this study
- •3. patients who take supplements or medical agents that consist with bifidobacteria, lactic acid bacteria, or galacto-oligosaccharide routinely, or patients who take yogurt (that includes lactic acid bacteria or Lactobacillus delbrueckii subsp. bulgaricus) or lactic acid bacteria beverage routinely for the purpose of intestinal regulation
- •4. patients with dementia
- •5. patients with alcoholism at giving their consent
- •6. patients who need legal representative for giving consent
- •7. patients with other conditions that the responsible investigator or subinvestigators think inappropriate to participate in the study
研究者
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