IRCT20131013014994N7尚未招募3 期
The effect of synbiotic supplementation on plasma levels of Advanced Glycation End Products and cardiovascular risk factors in hemodialysis patients: a double-blind clinical trial
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 入组人数
- 34
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
- no limit 至 no limit（—）
- 性别
- All
入选标准
- •Perform HD treatment at least twice a week for a maximum of 4 hours each time
- •Treatment under HD for at least 6 months
- •No pregnancy or breastfeeding
- •No immune system defects
- •No history of active cancers
- •No history of severe chronic diseases and acute medical conditions such as lung disease, cardiovascular disease, liver disease and acute pancreatitis
- •No addiction to alcohol or drugs
- •Lack of severe digestive disorders and diseases, HIV disease, mental problems
- •Ability to drink at least 200 ml of water per day
- •Life expectancy and survival for at least 3 months
- •Confirmation of written consent
排除标准
- •Patients with severe edema
- •People who had infection 4 weeks ago
- •People who took synbiotics, probiotics, prebiotics, or antibiotics during the 4 weeks before the study
- •Candidates for kidney and organ transplantation or peritoneal dialysis during 3 months of study
- •Taking immunosuppressive drugs or anticoagulants and chemotherapy drugs
- •Sensitivity to complementary compounds
- •The patient's unwillingness to participate in the study
- •Lack of complete answers to questions
- •Report side effects from taking synbiotics
研究者
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