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High Fiber in Parkinson's Disease

High Fiber in Parkinson's Disease

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04976959
Enrollment
60
Registered
2021-07-26
Start date
2021-07-08
Completion date
2025-08-31
Last updated
2024-02-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parkinson Disease

Brief summary

The purpose of the research is to determine the effects of a high-fiber nutritional supplement (HFS) on the bacteria, viruses, and fungi that live in different regions of the body in those with Parkinson's disease (PD). We will compare the bacteria, viruses, and fungi of those with PD to those without PD (healthy controls). We will also examine the effects of transplanting stool from humans into laboratory mice with or without Parkinson-like pathology to understand how the microbiome influences the brains of animals. We can use this information to get a better understanding of how changing the microbiome might help humans.

Interventions

DRUGHigh Fiber supplement

The supplement consists of a mixture of soluble fibers (from inulin and fibersol-2) and insoluble fibers (from oat bran, corn bran, wheat bran and sorghum bran) and it will be consumed as a drink.

Sponsors

Rutgers, The State University of New Jersey
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
50 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Parkinson's disease patients who are untreated

Exclusion criteria

* Occupation expected to change the microbiome (e.g. sanitation worker) * Treatment with medications that may induce parkinsonism (e.g. metoclopramide, typical or atypical antipsychotic agents) * Treatment within 12 weeks with oral or intravenous antibiotics * Known diagnosis of inflammatory bowel disease * Symptomatic organic gastrointestinal (GI) disease (other than hemorrhoids and hiatal hernia) or abdominal surgeries for symptomatic gastrointestinal disease such as bowel resection, diverticular surgery, colostomy; subjects with a history of an appendectomy or gallbladder removal for non-cancerous disease more than 5 years prior to presentation are allowed. * Symptomatic functional GI disease that significantly impairs intestinal motility such as scleroderma or use of GI motility drugs * Acute illness requiring immediate hospitalization * Pre-existent conditions as below: * Liver disease (cirrhosis or persistently abnormal AST or ALT that are 2X\> normal); * Kidney disease (creatinine\>2.0 mg/dL); * Uncontrolled psychiatric illness; * Clinically important lung disease or heart failure; * HIV disease; * Alcoholism, unreliable drinking history; or consumption of alcohol more than 3 times a week or binge drinking or drinking more than or equal to 3 drinks per occasion; * Transplant recipients; * Diabetes; * BMI \> 30 * Clinically significant dehydration or clinically detectable ascites or peripheral edema or cardiac failure * Presence of short bowel syndrome or severe malnutrition with ideal body weight \< or = 90% * Use of immunosuppressive medications in 3 months prior to enrollment * Anti-inflammatory medication use within 3 weeks of enrollment. * Chronic use of diuretics

Design outcomes

Primary

MeasureTime frame
changes in microbiome composition4 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026