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临床试验/NCT03348592
NCT03348592Unknown不适用

Gut Microbiome and p-Inulin in CKD TarGut CKD Study

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)1 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2016年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
18
试验地点
1
主要终点
Microbial composition of stool

研究概览

简要总结

The purpose of this Phase 1, 3-period crossover with repeated measures feasibility study is to characterize the gut microbiome of individuals with chronic kidney disease, and to explore effects of p-inulin on the gut microbiome. The nature of the study will provide information about the feasibility of stool sample collection for future multicenter studies of the gut microbiome.

详细描述

The overarching hypothesis motivating this exploratory study of variability is that treatment with oligofructose-enriched inulin (p-inulin) will alter the composition and/or function of the gut microbiome, and thereby reduce the generation of gut-derived uremic toxins, improve gut barrier function and attenuate systemic inflammation in CKD patients. In order to design a future clinical trial the following parameters from CKD subjects are needed:

  1. Intra-patient variability in the composition and function of the gut microbiome
  2. Inter-patient variability in the composition and function of the gut microbiome
  3. Impact of p-inulin on the composition and function of the gut microbiome
  4. Tolerability of p-inulin administration
  5. Feasibility of collecting stool samples in this patient population

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Subjects with eGFR 15.0 to 50.0 ml/min/1.73 m2 as estimated by the CKD-EPI equation
  • •Albuminuria greater than 300 mg/g creatinine (by spot urine test) if eGFR is ≥45 ml/min/1.73 m2
  • •Age ≥ 18 years
  • •For women of childbearing potential, willingness to use a highly effective method of birth control for up to 4 weeks after the last dose to study drug. See Section 4.2.1 for definition of childbearing potential and acceptable methods of birth control
  • •Ability to provide informed consent

排除标准

  • •Use of pre- or pro-biotics during the past 2 months
  • •Consumption of probiotic yogurt during the past 2 weeks
  • •Use of antibiotics within the past 3 months if the patient received a single course of antibiotic. If the patient received more than one course of antibiotic treatment, we will wait for 6 months prior to inclusion.
  • •Presence of HIV infection, chronic wound infection and osteomyelitis
  • •Presence of or treatment for periodontal infection
  • •Inflammatory bowel disease, chronic diarrhea, current C. difficile infection
  • •Cirrhosis or chronic active hepatitis
  • •Treatment with immunosuppressive medications in the past 6 months or more than a week of treatment with prednisone >10 mg in the last 3 months
  • •Treatment with proton pump inhibitors within the last one month
  • •Anticipated initiation of dialysis or kidney transplant within 9 months
  • •Acute on chronic kidney disease
  • •Expected survival < 9 months Do not disclose or use except as authorized by the Pilot Clinical Trials in CKD Consortium.
  • •Pregnancy, anticipated pregnancy, or breastfeeding
  • •Incarceration
  • •Participation in another intervention study
  • •Severe anemia defined as hemoglobin <9.0 g/dl any time during the last 3 months
  • •Patients in whom frequent blood sampling may be difficult

研究组 & 干预措施

Oligofructose-enriched inulin (p-inulin)

Experimental

Participants are on no treatment for 8 weeks, then the pre-biotic p-inulin for 12 weeks, then no treatment for 8 weeks. Inulin is derived from chicory root fiber. The dose is 16 grams of p-inulin powder per day.

干预措施: Oligofructose-enriched inulin (p-inulin) (Dietary Supplement)

Oligofructose-enriched inulin (p-inulin)

Experimental

Participants are on no treatment for 8 weeks, then the pre-biotic p-inulin for 12 weeks, then no treatment for 8 weeks. Inulin is derived from chicory root fiber. The dose is 16 grams of p-inulin powder per day.

干预措施: No treatment (Other)

结局指标

主要结局

Microbial composition of stool

时间窗: Stool is collected weekly for 28 weeks

Microbial taxonomy will be assigned using Ribosomal Database Project (RDP) for 16S, augmented by analysis of specific sequences using BLAST. The 16S tag sequences will be collected into operational taxonomic units (OTUs) with 97% sequence identity.

Adherence to p inulin prescription

时间窗: Packets are counted every four weeks during the 12 weeks when the patient is taking p inulin

Proportion of packets taken vs packets prescribed by packet count

次要结局

  • Allantoin(collected weekly for 28 weeks)
  • Indoles(collected weekly for 28 weeks)
  • Phenols(collected weekly for 28 weeks)
  • Fructose(collected weekly for 28 weeks)
  • Cytokines(collected weekly for 28 weeks)
  • endotoxin(collected weekly for 28 weeks)
  • TNF-R1(collected weekly for 28 weeks)
  • Lipopolysaccharide binding protein (LBP)(collected weekly for 28 weeks)
  • sCD14(collected weekly for 28 weeks)
  • butyrate(Collected weekly for 28 weeks)
  • Choline(Collected weekly for 28 weeks)
  • Betaine(Collected weekly for 28 weeks)
  • metabolites of urea and creatinine metabolism(collected weekly for 28 weeks)
  • Myeloperoxdase (MPO)(collected weekly for 28 weeks)
  • HMGB1(collected weekly for 28 weeks)
  • propionate(Collected weekly for 28 weeks)
  • acetate(Collected weekly for 28 weeks)
  • Trimethylamine N oxide(Collected weekly for 28 weeks)
  • polyamines(collected weekly for 28 weeks)
  • hsCRP(collected weekly for 28 weeks)
  • TNF-R2(collected weekly for 28 weeks)

研究者

申办方类型
Nih
责任方
Principal Investigator
主要研究者

Jennifer Gassman

Principal Investigator - Data Coordinating Center

The Cleveland Clinic

研究点 (1)

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