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The Use of A Prebiotic to Promote a Healthy Gut Microbiome in Pediatric Stem Cell Transplant Recipients

Primary Purpose

Microbial Colonization

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Prebiotics
Placebos
Sponsored by
Ann & Robert H Lurie Children's Hospital of Chicago
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Microbial Colonization focused on measuring Microbiome, Prebiotic

Eligibility Criteria

2 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age 2-18 years
  2. Allogeneic Stem Cell transplant
  3. Myeloablative therapy
  4. Inpatient at Lurie Children's Hospital

Exclusion Criteria:

  1. Previous Hematopoietic Stem Cell Transplant
  2. Autologous Stem Cell Transplant
  3. Reduced Intensity Conditioning used for transplant
  4. History of ulcerative colitis, Crohn's disease, irritable bowel syndrome, celiac disease
  5. History of Type 1 or Type 2 Diabetes Mellitus
  6. Previous abdominal surgery necessitating the use of an ostomy
  7. G-tube dependence
  8. Nasal gastric/oral gastric tube dependence prior to starting the conditioning process
  9. Graft vs host disease prior to enrollment at any site
  10. 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

Sites / Locations

  • Ann & Robert H Lurie Children's Hospital of ChicagoRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Placebo Arm

Prebiotic (Inulin) Arm

Arm Description

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)

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)

Outcomes

Primary Outcome Measures

Change in alpha and beta bacterial diversity measures in stool
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
Compare the effect of oral inulin vs. placebo on SCFA levels in the stool of children undergoing hematopoietic stem cell transplant

Secondary Outcome Measures

Bacterial Resistance genes in stool
Determine the impact of inulin intake vs. placebo on the prevalence of genes associated with antibiotic resistance of children undergoing hematopoietic stem cell transplant

Full Information

First Posted
June 25, 2019
Last Updated
February 20, 2020
Sponsor
Ann & Robert H Lurie Children's Hospital of Chicago
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1. Study Identification

Unique Protocol Identification Number
NCT04111471
Brief Title
The Use of A Prebiotic to Promote a Healthy Gut Microbiome in Pediatric Stem Cell Transplant Recipients
Official Title
The Use of Inulin to Prevent Dysbiosis in Pediatric Hematopoietic Stem Cell Transplant Recipients
Study Type
Interventional

2. Study Status

Record Verification Date
February 2020
Overall Recruitment Status
Unknown status
Study Start Date
October 31, 2019 (Actual)
Primary Completion Date
March 2021 (Anticipated)
Study Completion Date
July 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ann & Robert H Lurie Children's Hospital of Chicago

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Microbial Colonization
Keywords
Microbiome, Prebiotic

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Qualified patients that are admitted to Lurie Children's Hospital and agree to participate will either be randomized to receive the placebo or prebiotic, inulin. Randomization will occur 1:1
Masking
ParticipantCare ProviderInvestigator
Masking Description
Participants will be randomized by an independent statistician based on patient enrollment number (LCH 001- LCH 040). Randomization will be 1:1. The statistician will randomly assort LCH 001-020 into Inulin/Placebo and LCH 021- LCH 040 into Inulin/placebo. This will ensure that an equal number of enrolled participants will be in each arm at 20 patients, and then again at anticipated full 40 patients
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Placebo Arm
Arm Type
Placebo Comparator
Arm Description
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)
Arm Title
Prebiotic (Inulin) Arm
Arm Type
Experimental
Arm Description
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)
Intervention Type
Drug
Intervention Name(s)
Prebiotics
Other Intervention Name(s)
inulin
Intervention Description
Enrolled patients will receive 10 grams of inulin daily for 21 days
Intervention Type
Drug
Intervention Name(s)
Placebos
Other Intervention Name(s)
Maltodextrin
Intervention Description
Enrolled patients will receive 5.6 grams of placebo powder daily for 21 days
Primary Outcome Measure Information:
Title
Change in alpha and beta bacterial diversity measures in stool
Description
Compare the effect of oral inulin vs. placebo on alpha and beta bacterial diversity in the stool of children undergoing hematopoietic stem cell transplant
Time Frame
Change of baseline alpha and beta bacterial diversity at 100 days after transplant
Title
Change in Short Chain Fatty Acid (SCFA) levels in stool
Description
Compare the effect of oral inulin vs. placebo on SCFA levels in the stool of children undergoing hematopoietic stem cell transplant
Time Frame
Change in baseline SCFA levels in stool at 100 days after transplant
Secondary Outcome Measure Information:
Title
Bacterial Resistance genes in stool
Description
Determine the impact of inulin intake vs. placebo on the prevalence of genes associated with antibiotic resistance of children undergoing hematopoietic stem cell transplant
Time Frame
Measured at enrollment, on the day of transplant, 30 days after transplant, and near 100 days after transplant

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 2-18 years Allogeneic Stem Cell transplant Myeloablative therapy Inpatient at Lurie Children's Hospital Exclusion Criteria: 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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Alexander M Newman, MD
Phone
3122274080
Email
anewman@luriechildrens.org
First Name & Middle Initial & Last Name or Official Title & Degree
Mehreen Arshad, MD
Phone
3122274080
Email
MArshad@luriechildrens.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alexander M Newman, MD
Organizational Affiliation
Lurie Children's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ann & Robert H Lurie Children's Hospital of Chicago
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Individual Site Status
Recruiting

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

The Use of A Prebiotic to Promote a Healthy Gut Microbiome in Pediatric Stem Cell Transplant Recipients

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