The Use of A Prebiotic to Promote a Healthy Gut Microbiome in Pediatric Stem Cell Transplant Recipients
- Conditions
- Microbial Colonization
- Interventions
- Drug: PlacebosDrug: Prebiotics
- Registration Number
- NCT04111471
- Brief Summary
This study will look at the effect of the prebiotic inulin compared to placebo on children undergoing stem cell transplant.
- Detailed Description
Children enrolled in the study will receive either the prebiotic inulin or a placebo for 21 days during the study period. They will start taking the product seven days before transplant starts until 14 days after transplant. Stool will be collected twice weekly until thirty days after transplant or discharge, whichever occurs first. Stool samples will be sampled for metagenomic sequencing to identify the diversity of bacteria within the stool. They will also be analyzed for amount of short-chain fatty acid content (a breakdown product of inulin) as well as for presence of genes that confer antibiotic resistance. From 30 days after transplant until 100 days after transplant, two stool samples will be collected at regularly scheduled follow up appointments (near day 60 and day 100). No product (inulin or placebo) will be given during this time frame. The study period ends 100 days after transplant.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 5
- Age 2-18 years
- Allogeneic Stem Cell transplant
- Myeloablative therapy
- Inpatient at Lurie Children's Hospital
- Previous Hematopoietic Stem Cell Transplant
- Autologous Stem Cell Transplant
- Reduced Intensity Conditioning used for transplant
- History of ulcerative colitis, Crohn's disease, irritable bowel syndrome, celiac disease
- History of Type 1 or Type 2 Diabetes Mellitus
- Previous abdominal surgery necessitating the use of an ostomy
- G-tube dependence
- Nasal gastric/oral gastric tube dependence prior to starting the conditioning process
- Graft vs host disease prior to enrollment at any site
- Children under 2 years of age - literature shows that the microbiome is still developing in children under two years of age, and this development may skew results
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Placebo Arm Placebos 20 patients will receive 5.6 g of placebo product (maltodextrin) daily for a total of 21 days (7 days before and until 2 weeks after transplant) Prebiotic (Inulin) Arm Prebiotics 20 patients will receive 10 g of inulin product daily for a total of 21 days (7 days before and until 2 weeks after transplant)
- Primary Outcome Measures
Name Time Method Change in alpha and beta bacterial diversity measures in stool Change of baseline alpha and beta bacterial diversity at 100 days after transplant Compare the effect of oral inulin vs. placebo on alpha and beta bacterial diversity in the stool of children undergoing hematopoietic stem cell transplant
Change in Short Chain Fatty Acid (SCFA) levels in stool Change in baseline SCFA levels in stool at 100 days after transplant Compare the effect of oral inulin vs. placebo on SCFA levels in the stool of children undergoing hematopoietic stem cell transplant
- Secondary Outcome Measures
Name Time Method Bacterial Resistance genes in stool Measured at enrollment, on the day of transplant, 30 days after transplant, and near 100 days after transplant Determine the impact of inulin intake vs. placebo on the prevalence of genes associated with antibiotic resistance of children undergoing hematopoietic stem cell transplant
Trial Locations
- Locations (1)
Ann & Robert H Lurie Children's Hospital of Chicago
🇺🇸Chicago, Illinois, United States