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Resistant Maltodextrin for Gut Microbiome in Parkinson's Disease: Safety and Tolerability Study

Primary Purpose

Parkinson Disease, Intestinal Bacteria Flora Disturbance, Dietary Modification

Status
Active
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Resistant maltodextrin
maltodextrin
Sponsored by
Northwestern University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Parkinson Disease focused on measuring Resistant maltodextrin, dietary fiber, gut microbiome, Parkinson's disease

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Men and women age ≥60 years
  • Diagnosis of PD based on United Kingdom PD brain bank criteria, Hoehn and Yahr stage 1-3.
  • Stable dose of PD medications for 30 days prior to study and for duration of study
  • If used, stable dose of melatonin, sedative/hypnotic or stimulant medications

Exclusion Criteria:

  • use of other prebiotic or probiotic treatment for 30 days prior to or during the study
  • unstable medical or psychiatric disorder
  • history of diabetes mellitus or current use of medication for diabetes
  • cognitive impairment based on Montreal Cognitive Assessment (MoCA) <25.
  • current or recent (within previous 3 weeks) use of laxatives
  • use of antibiotics in the past 30 days
  • participation in another clinical trial in the past 30 days.

Sites / Locations

  • Northwestern University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Resistant Maltodextrin

Maltodextrin

Arm Description

Resistant maltodextrin (RM) powder 25 g during days 1-7 and 50g during days 8-28, each dose dissolved in 8 oz of water once daily in the morning.

Maltodextrin 25g for days 1-7 and 50 g for days 8-28, each dose dissolved in 8 oz of water once daily in the morning.

Outcomes

Primary Outcome Measures

Adverse events
Adverse event frequency and severity based on diary reports, phone calls, and in-person assessments.

Secondary Outcome Measures

Gut microbial remodeling
Change in fecal butyrate-producing bacteria based on high-throughput amplicon sequencing of the V4 variable region of the microbial 16s ribosomal ribonucleic acid (RNA) gene.

Full Information

First Posted
September 10, 2018
Last Updated
January 13, 2023
Sponsor
Northwestern University
Collaborators
University of Illinois at Chicago
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1. Study Identification

Unique Protocol Identification Number
NCT03667404
Brief Title
Resistant Maltodextrin for Gut Microbiome in Parkinson's Disease: Safety and Tolerability Study
Official Title
Gut Microbial Remodeling With Resistant Maltodextrin for Motor and Non-motor Symptoms in Parkinson's Disease: Safety and Tolerability Study
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
November 6, 2018 (Actual)
Primary Completion Date
June 30, 2022 (Actual)
Study Completion Date
June 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Northwestern University
Collaborators
University of Illinois at 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
This study will evaluate the safety and tolerability of a dietary fiber, resistant maltodextrin, in people with Parkinson's disease. It will also evaluate the fiber's effect on the gut microbiome and potential effects on motor function and non-motor functions. Half of the participants will receive resistant maltodextrin and the other half will receive a control substance, maltodextrin.
Detailed Description
Intestinal microbiota may play in important role in Parkinson's disease (PD). Colonic bacteria play roles in multiple functions including gut motility and secretion of metabolites which can have systemic effects on the body. Recent evidence has shown that people with PD have an altered distribution of gut bacteria that healthy controls. These changes are associated with differences in various metabolites, including butyrate, that are involved in maintaining the gut barrier integrity and even gait and balance function. Microbiota dysbiosis could potentially exacerbate or even contribute to the pathogenesis of PD. Probiotic and dietary interventions may improve gut function and the motor symptoms in PD, but neither have been examined for their effect on the gut microbiome. Prebiotic treatments have been shown to order the microbiome in some populations, but have not been assessed for tolerability or efficacy in PD. The objective of this study is to examine the safety and tolerability of resistant maltodextrin (RM), a prebiotic non-digestible fiber, and its effect on the microbiome and motor in non-motor symptoms and PD. The investigators will conduct a randomized, parallel-group double-blinded controlled trial assessing RM 50 g daily compared to maltodextrin (an easily digestible glucose polysaccharide) over 4 weeks. Patients will be dosed with 25 g daily for 1 week and then titrated to 50 g daily for the remaining 3 weeks. The goals of this study include: 1) To determine the safety and tolerability of RM compared to maltodextrin in patients with PD; 2) To determine if RM will remodel the gut microbiome in patients with PD; 3) (exploratory) To determine if RM administration will improve motor and non-motor symptoms in PD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson Disease, Intestinal Bacteria Flora Disturbance, Dietary Modification
Keywords
Resistant maltodextrin, dietary fiber, gut microbiome, Parkinson's disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Double blind placebo (maltodextrin) controlled randomized trial
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
participants will be blinded to condition. control condition (maltodextrin) will be used and has identical appearance. investigator and research staff (except pharmacy) will be blinded to condition
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Resistant Maltodextrin
Arm Type
Experimental
Arm Description
Resistant maltodextrin (RM) powder 25 g during days 1-7 and 50g during days 8-28, each dose dissolved in 8 oz of water once daily in the morning.
Arm Title
Maltodextrin
Arm Type
Placebo Comparator
Arm Description
Maltodextrin 25g for days 1-7 and 50 g for days 8-28, each dose dissolved in 8 oz of water once daily in the morning.
Intervention Type
Dietary Supplement
Intervention Name(s)
Resistant maltodextrin
Intervention Description
Resistant maltodextrin powder
Intervention Type
Dietary Supplement
Intervention Name(s)
maltodextrin
Intervention Description
maltodextrin powder
Primary Outcome Measure Information:
Title
Adverse events
Description
Adverse event frequency and severity based on diary reports, phone calls, and in-person assessments.
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Gut microbial remodeling
Description
Change in fecal butyrate-producing bacteria based on high-throughput amplicon sequencing of the V4 variable region of the microbial 16s ribosomal ribonucleic acid (RNA) gene.
Time Frame
4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men and women age ≥60 years Diagnosis of PD based on United Kingdom PD brain bank criteria, Hoehn and Yahr stage 1-3. Stable dose of PD medications for 30 days prior to study and for duration of study If used, stable dose of melatonin, sedative/hypnotic or stimulant medications Exclusion Criteria: use of other prebiotic or probiotic treatment for 30 days prior to or during the study unstable medical or psychiatric disorder history of diabetes mellitus or current use of medication for diabetes cognitive impairment based on Montreal Cognitive Assessment (MoCA) <25. current or recent (within previous 3 weeks) use of laxatives use of antibiotics in the past 30 days participation in another clinical trial in the past 30 days.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Roneil G Malkani
Organizational Affiliation
Northwestern Feinberg School of Medicine Department of Neurology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwestern University
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
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Resistant Maltodextrin for Gut Microbiome in Parkinson's Disease: Safety and Tolerability Study

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