search
Back to results

GPR109A and Parkinson's Disease: Role of Niacin in Outcome Measures

Primary Purpose

Parkinson's Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
niacin
placebo
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Parkinson's Disease

Eligibility Criteria

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

Inclusion Criteria:

  • PD subjects will be adult men and women diagnosed with idiopathic mild to moderately severe PD defined as modified Hoehn & Yahr Stages I-III (while "On").

    • PD is defined according to the United Kingdom Brain Bank Criteria made at least six months prior to recruitment to the study.
    • PD features include the presence of at least two of the four cardinal clinical manifestations of the disease, which are tremor, rigidity, bradykinesia, and disturbances of posture or gait, without any other known or suspected cause of Parkinsonism.
  • Subjects should be stabilized on PD medication for at least 3 months before enrollment into the study.
  • Subjects' PD drug prescriptions will not be altered nor withheld during the study, i.e., they will be tested while "On."
  • The patient will have signed informed consent.
  • Subjects who do not have PD (i.e., healthy or have other medical conditions such as traumatic brain injury (TBI), stroke, or other syndromes in which inflammation plays a role in the condition) will also be recruited as control subjects.
  • This will allow us to estimate whether these other conditions show similar or unique inflammatory profile.

Exclusion Criteria:

  • Subjects will be excluded if they had previous brain surgery or other severe neurological problems

    • intracerebral hemorrhage
    • traumatic brain injury
    • central nervous system malignancy
    • active central nervous system (CNS) infection
    • significant stroke
    • Alzheimer disease or any type of implanted stimulator including but not limited to Deep Brain Stimulator (DBS) or pacemaker
  • All subjects must be without evidence of dementia, defined as a score > 24 the Mini-Mental State Examination and able to understand test instructions
  • Subjects must not have functional blindness (inability to participate in gait and visuomotor assessments) or lower limb amputation higher than the forefoot or any orthopedic problem that precludes performance of physical tests
  • Allergic to niacin
  • Significant cardiac, pulmonary, hepatic, gastrointestinal, or renal disease

    • e.g., New York Heart Association Class III or IV congestive heart failure
    • endocarditis
    • pulmonary insufficiency symptomatic at rest or with mild physical exertion
    • acute or chronic hepatitis
    • renal failure requiring dialysis
    • second and third degree atrioventricular block or sick sinus syndrome), or diabetes are also exclusionary factors

Sites / Locations

  • Charlie Norwood VA Medical Center, Augusta, GA

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

niacin

placebo

Arm Description

Niacin 250 mg is compared to placebo tablet.

placebo

Outcomes

Primary Outcome Measures

Unified Parkinson's Disease Rating Scale (UPDRS) Change
This is the Unified Parkinson's disease rating scale assessment. The investigators assess I, II, III and V components of the UPDRS. UPDRS 3 is motor skills. Higher scores mean worse outcome. A 0 is minimum and 120 is the maximum.
REM Sleep Pattern
This requires an instrument Zeo sleep monitor. Subjects are given instructions how to use it. Sleep sensor patches are supposed to be applied on forehead before going to sleep and the data of quality of sleep is captured overnight. The reported data captures the rapid eye movement (REM) sleep as a percentage.
Deep Sleep
This requires an instrument Zeo sleep monitor. Subjects are given instructions how to use it. Sleep sensor patches are supposed to be applied on forehead before going to sleep and the data of quality of sleep is captured overnight. The reported data captures the deep sleep percentage.
Light Sleep
This requires an instrument Zeo sleep monitor. Subjects are given instructions how to use it. Sleep sensor patches are supposed to be applied on forehead before going to sleep and the data of quality of sleep is captured overnight. The reported data captures the light sleep percentage.
Sleep Time - Awake
This requires an instrument Zeo sleep monitor. Subjects are given instructions how to use it. Sleep sensor patches are supposed to be applied on forehead before going to sleep and the data of quality of sleep is captured overnight. The reported data captures the awake time during night sleep percentage.
Mini-Mental State Examination (MMSE) Change
It captures mental status and awareness of time, place and surrounding. A zero is minimum and 30 is maximum. Higher score indicates better cognition.
Stroop Test Change
It captures understanding of color and its description within a certain time frame when letters and colors do not match. There are only two choices to pick from and the correct choices should be made to proceed to the next one. Correct choices are given one point and incorrect choices delete one point. Maximum number of correct choices per unit time are recorded. Three initial trials are given to understand the test. No minimum or maximum values. Higher numbers indicate better cognition.
Fatigue Severity Scale
Fatigue was rated from 0-7 in a fatigue questionnaire. A 0 being the least and 7 being the highest level of fatigue.

Secondary Outcome Measures

Cerebrospinal Fluid Changes - Interleukin 6 (IL6)
IL-6 cytokine levels will be tested in cerebral spinal fluid (CSF) at baseline and 6 months after intervention.
Cerebrospinal Fluid Changes - Interleukin 10 (IL-10)
IL-10 will be tested in cerebral spinal fluid (CSF) at baseline and 6 months after intervention.
Niacin Metabolite in Urine - Niacin
Plasma and urine samples will be tested to report levels of niacin and its metabolites. Higher value indicates higher niacin levels
Niacin Metabolites in Urine - NAM Nicotinamide
Plasma and urine samples will be tested to report levels of niacin and its metabolites. Higher value indicates higher niacin levels
Niacin Changes in Plasma - Niacin
Plasma and urine samples will be tested to report levels of niacin and its metabolites. Higher value indicates higher niacin levels.
Niacin Changes in Plasma - NUA Nicotinuric Acid
Plasma and urine samples will be tested to report levels of niacin and its metabolites. Higher value indicates higher niacin levels
Cerebrospinal Fluid Changes - Interleukin 8 (IL8)
IL-8 cytokine levels will be tested in cerebral spinal fluid (CSF) at baseline and 6 months after intervention.
Niacin Metabolite in Urine - Nicotinuric Acid NUA
Plasma and urine samples will be tested to report levels of niacin and its metabolites. Higher value indicates higher niacin levels
CSF Fluid Changes - Interleukin 1B (IL-1B)
IL-1beta levels were tested in cerebral spinal fluid (CSF) at baseline and 6 months after intervention.
Cerebrospinal Fluid (CSF) Changes - Macrophage Inflammatory Protein 1 Beta (MIP 1 Beta)
Inflammatory and non-inflammatory cytokines levels will be tested in cerebral spinal fluid (CSF) at baseline and 6 months after intervention. We are reporting levels of MIP-1 beta here.
Macrophage Changes
The blood is tested to report G-protein coupled receptor 109A (GPR109A) levels in macrophages in M1 and M2 populations.
Niacin Metabolite Changes in Plasma - Nicotinamide (NAM)
Plasma and urine samples will be tested to report levels of niacin and its metabolites. Higher value indicates higher niacin levels.
CSF Changes in Interferon Gamma (IF-gamma)
Inflammatory and non-inflammatory cytokines levels will be tested in cerebral spinal fluid (CSF) at baseline and 6 months after intervention. We are reporting levels of IF-gamma beta here.
CSF Changes - Tumor Necrosis Factor - Alpha (TNF-alpha)
Inflammatory and non-inflammatory cytokines levels will be tested in cerebral spinal fluid (CSF) at baseline and 6 months after intervention. We are reporting levels of TNF-alpha here.
Cerebral Spinal Fluid Changes - Interferon Gamma Induced Protein -10 (IP-10)
Inflammatory and non-inflammatory cytokines levels will be tested in cerebral spinal fluid (CSF) at baseline and 6 months after intervention. We are reporting levels of IP-10 here.
Cerebral Spinal Fluid (CSF) Changes - Monocyte Chemoattractant Protein 4 (MCP4)
Inflammatory and non-inflammatory cytokines levels will be tested in cerebral spinal fluid (CSF) at baseline and 6 months after intervention. We are reporting levels of MCP4 here.
Cerebral Spinal Fluid (CSF) Changes - MIP1-alpha
Inflammatory and non-inflammatory cytokines levels will be tested in cerebral spinal fluid (CSF) at baseline and 6 months after intervention. We are reporting levels of MIP1-alpha here.
Plasma Cytokines - IF Gamma
Inflammatory and non-inflammatory cytokines levels will be tested in plasma at baseline and 6 months after intervention. We are reporting levels of IF-gamma here.
Plasma Cytokines - IL-10
Inflammatory and non-inflammatory cytokines levels will be tested in plasma at baseline and 6 months after intervention. We are reporting levels of IL-10 here.
Plasma Cytokines - IL1-B
Inflammatory and non-inflammatory cytokines levels will be tested in plasma at baseline and 6 months after intervention. We are reporting levels of IL-1B here.
Plasma Cytokines - IL-6
Inflammatory and non-inflammatory cytokines levels will be tested in plasma at baseline and 6 months after intervention. We are reporting levels of IL-6 here.
Plasma Cytokines - IL-8
Inflammatory and non-inflammatory cytokines levels will be tested in plasma at baseline and 6 months after intervention. We are reporting levels of IL-8 here.
Plasma Cytokines - TNF-alpha
Inflammatory and non-inflammatory cytokines levels will be tested in plasma at baseline and 6 months after intervention. We are reporting levels of TNF-alpha here.
Plasma Cytokines - IP-10
Inflammatory and non-inflammatory cytokines levels will be tested in plasma at baseline and 6 months after intervention. We are reporting levels of IP-10 here.
Plasma Cytokines - MCP-4
Inflammatory and non-inflammatory cytokines levels will be tested in plasma at baseline and 6 months after intervention. We are reporting levels of MCP-4 here.
Plasma Cytokines - MIP1-alpha
Inflammatory and non-inflammatory cytokines levels will be tested in plasma at baseline and 6 months after intervention. We are reporting levels of MIP1-alpha here.
Plasma Cytokines - MIP1-beta
Inflammatory and non-inflammatory cytokines levels will be tested in plasma at baseline and 6 months after intervention. We are reporting levels of MIP1-beta here.
Plasma Levels - Serotonin
Plasma serotonin levels

Full Information

First Posted
February 22, 2018
Last Updated
October 18, 2021
Sponsor
VA Office of Research and Development
search

1. Study Identification

Unique Protocol Identification Number
NCT03462680
Brief Title
GPR109A and Parkinson's Disease: Role of Niacin in Outcome Measures
Official Title
GPR109A and Parkinson's Disease: Role of Niacin in Outcome Measures
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
September 28, 2016 (Actual)
Primary Completion Date
April 23, 2020 (Actual)
Study Completion Date
April 23, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Inflammation plays a central role in Parkinson's disease. The use of anti-inflammatory drugs was found to reduce the risk of PD . Niacin may play an important role in reducing inflammation in PD. The investigators also found that individuals with PD have a chronic niacin deficiency . The purposes of this study are to (1) examine the blood, urine and spinal fluid of persons with Parkinson's to look for evidence of inflammation and; (2) whether 6 months of vitamin B3 supplements may reduce the inflammation and/or improve symptoms.
Detailed Description
Inflammation plays a central role in Parkinson's disease (PD) pathology [1] as evidenced by the presence of microglia in the substantia nigra in post-mortem samples [2] as well as activated microglia and cytokines in clinical and animal studies [3]. The use of non-aspirin non-steroidal anti-inflammatory drugs was found to reduce the risk of PD [4]. The investigators recently identified an anti-inflammatory receptor GPR109A that is upregulated in PD [5]. Niacin has a high affinity for this receptor, suggesting that it (niacin) may play an important role in reducing inflammation in PD. The investigators also found that individuals with PD have a chronic niacin deficiency [5]. Using seed funding from the local PD chapter, the investigators obtained pilot data which suggested that restoring the deficiency via over-the-counter (OTC) supplementation reduced inflammation and decreased the severity of the disease symptoms [6]. In this VA-funded study, the investigators will determine the effect of 6 months' OTC niacin supplementation on inflammation (as assessed in the blood and spinal fluid) and severity of the PD symptoms.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson's Disease

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
There are two arms, niacin and placebo. They are double blind and randomized.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Only Pharmacists keep the log of the drug dispensed. Everyone else is blinded.
Allocation
Randomized
Enrollment
47 (Actual)

8. Arms, Groups, and Interventions

Arm Title
niacin
Arm Type
Active Comparator
Arm Description
Niacin 250 mg is compared to placebo tablet.
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
placebo
Intervention Type
Dietary Supplement
Intervention Name(s)
niacin
Other Intervention Name(s)
vitamin B3
Intervention Description
Niacin or nicotinic acid 250 mg tablets
Intervention Type
Other
Intervention Name(s)
placebo
Intervention Description
placebo tablet
Primary Outcome Measure Information:
Title
Unified Parkinson's Disease Rating Scale (UPDRS) Change
Description
This is the Unified Parkinson's disease rating scale assessment. The investigators assess I, II, III and V components of the UPDRS. UPDRS 3 is motor skills. Higher scores mean worse outcome. A 0 is minimum and 120 is the maximum.
Time Frame
at the recruitment and after 6 months
Title
REM Sleep Pattern
Description
This requires an instrument Zeo sleep monitor. Subjects are given instructions how to use it. Sleep sensor patches are supposed to be applied on forehead before going to sleep and the data of quality of sleep is captured overnight. The reported data captures the rapid eye movement (REM) sleep as a percentage.
Time Frame
baseline and after 6 months
Title
Deep Sleep
Description
This requires an instrument Zeo sleep monitor. Subjects are given instructions how to use it. Sleep sensor patches are supposed to be applied on forehead before going to sleep and the data of quality of sleep is captured overnight. The reported data captures the deep sleep percentage.
Time Frame
At baseline and after 6 months
Title
Light Sleep
Description
This requires an instrument Zeo sleep monitor. Subjects are given instructions how to use it. Sleep sensor patches are supposed to be applied on forehead before going to sleep and the data of quality of sleep is captured overnight. The reported data captures the light sleep percentage.
Time Frame
baseline and 6 months
Title
Sleep Time - Awake
Description
This requires an instrument Zeo sleep monitor. Subjects are given instructions how to use it. Sleep sensor patches are supposed to be applied on forehead before going to sleep and the data of quality of sleep is captured overnight. The reported data captures the awake time during night sleep percentage.
Time Frame
at baseline and 6 months
Title
Mini-Mental State Examination (MMSE) Change
Description
It captures mental status and awareness of time, place and surrounding. A zero is minimum and 30 is maximum. Higher score indicates better cognition.
Time Frame
at baseline and after 6 months of treatment
Title
Stroop Test Change
Description
It captures understanding of color and its description within a certain time frame when letters and colors do not match. There are only two choices to pick from and the correct choices should be made to proceed to the next one. Correct choices are given one point and incorrect choices delete one point. Maximum number of correct choices per unit time are recorded. Three initial trials are given to understand the test. No minimum or maximum values. Higher numbers indicate better cognition.
Time Frame
at the baseline and after 6 months of intervention
Title
Fatigue Severity Scale
Description
Fatigue was rated from 0-7 in a fatigue questionnaire. A 0 being the least and 7 being the highest level of fatigue.
Time Frame
at baseline and after 6 months
Secondary Outcome Measure Information:
Title
Cerebrospinal Fluid Changes - Interleukin 6 (IL6)
Description
IL-6 cytokine levels will be tested in cerebral spinal fluid (CSF) at baseline and 6 months after intervention.
Time Frame
at baseline and after 6 months
Title
Cerebrospinal Fluid Changes - Interleukin 10 (IL-10)
Description
IL-10 will be tested in cerebral spinal fluid (CSF) at baseline and 6 months after intervention.
Time Frame
at baseline and after 6 months
Title
Niacin Metabolite in Urine - Niacin
Description
Plasma and urine samples will be tested to report levels of niacin and its metabolites. Higher value indicates higher niacin levels
Time Frame
at baseline and after 6 months
Title
Niacin Metabolites in Urine - NAM Nicotinamide
Description
Plasma and urine samples will be tested to report levels of niacin and its metabolites. Higher value indicates higher niacin levels
Time Frame
at baseline and 6 months
Title
Niacin Changes in Plasma - Niacin
Description
Plasma and urine samples will be tested to report levels of niacin and its metabolites. Higher value indicates higher niacin levels.
Time Frame
baseline and 6 months
Title
Niacin Changes in Plasma - NUA Nicotinuric Acid
Description
Plasma and urine samples will be tested to report levels of niacin and its metabolites. Higher value indicates higher niacin levels
Time Frame
at baseline and 6 months
Title
Cerebrospinal Fluid Changes - Interleukin 8 (IL8)
Description
IL-8 cytokine levels will be tested in cerebral spinal fluid (CSF) at baseline and 6 months after intervention.
Time Frame
at baseline and after 6 months
Title
Niacin Metabolite in Urine - Nicotinuric Acid NUA
Description
Plasma and urine samples will be tested to report levels of niacin and its metabolites. Higher value indicates higher niacin levels
Time Frame
at baseline and after 6 months
Title
CSF Fluid Changes - Interleukin 1B (IL-1B)
Description
IL-1beta levels were tested in cerebral spinal fluid (CSF) at baseline and 6 months after intervention.
Time Frame
at baseline and 6 months
Title
Cerebrospinal Fluid (CSF) Changes - Macrophage Inflammatory Protein 1 Beta (MIP 1 Beta)
Description
Inflammatory and non-inflammatory cytokines levels will be tested in cerebral spinal fluid (CSF) at baseline and 6 months after intervention. We are reporting levels of MIP-1 beta here.
Time Frame
at baseline and after 6 months
Title
Macrophage Changes
Description
The blood is tested to report G-protein coupled receptor 109A (GPR109A) levels in macrophages in M1 and M2 populations.
Time Frame
at baseline and after 6 months
Title
Niacin Metabolite Changes in Plasma - Nicotinamide (NAM)
Description
Plasma and urine samples will be tested to report levels of niacin and its metabolites. Higher value indicates higher niacin levels.
Time Frame
at baseline and after 6 months
Title
CSF Changes in Interferon Gamma (IF-gamma)
Description
Inflammatory and non-inflammatory cytokines levels will be tested in cerebral spinal fluid (CSF) at baseline and 6 months after intervention. We are reporting levels of IF-gamma beta here.
Time Frame
at baseline and after 6 months
Title
CSF Changes - Tumor Necrosis Factor - Alpha (TNF-alpha)
Description
Inflammatory and non-inflammatory cytokines levels will be tested in cerebral spinal fluid (CSF) at baseline and 6 months after intervention. We are reporting levels of TNF-alpha here.
Time Frame
at baseline and after 6 months
Title
Cerebral Spinal Fluid Changes - Interferon Gamma Induced Protein -10 (IP-10)
Description
Inflammatory and non-inflammatory cytokines levels will be tested in cerebral spinal fluid (CSF) at baseline and 6 months after intervention. We are reporting levels of IP-10 here.
Time Frame
at baseline and after 6 months
Title
Cerebral Spinal Fluid (CSF) Changes - Monocyte Chemoattractant Protein 4 (MCP4)
Description
Inflammatory and non-inflammatory cytokines levels will be tested in cerebral spinal fluid (CSF) at baseline and 6 months after intervention. We are reporting levels of MCP4 here.
Time Frame
at baseline and after 6 months
Title
Cerebral Spinal Fluid (CSF) Changes - MIP1-alpha
Description
Inflammatory and non-inflammatory cytokines levels will be tested in cerebral spinal fluid (CSF) at baseline and 6 months after intervention. We are reporting levels of MIP1-alpha here.
Time Frame
at baseline and after 6 months
Title
Plasma Cytokines - IF Gamma
Description
Inflammatory and non-inflammatory cytokines levels will be tested in plasma at baseline and 6 months after intervention. We are reporting levels of IF-gamma here.
Time Frame
at baseline and after 6 months
Title
Plasma Cytokines - IL-10
Description
Inflammatory and non-inflammatory cytokines levels will be tested in plasma at baseline and 6 months after intervention. We are reporting levels of IL-10 here.
Time Frame
at baseline and after 6 months
Title
Plasma Cytokines - IL1-B
Description
Inflammatory and non-inflammatory cytokines levels will be tested in plasma at baseline and 6 months after intervention. We are reporting levels of IL-1B here.
Time Frame
at baseline and after 6 months
Title
Plasma Cytokines - IL-6
Description
Inflammatory and non-inflammatory cytokines levels will be tested in plasma at baseline and 6 months after intervention. We are reporting levels of IL-6 here.
Time Frame
at baseline and after 6 months
Title
Plasma Cytokines - IL-8
Description
Inflammatory and non-inflammatory cytokines levels will be tested in plasma at baseline and 6 months after intervention. We are reporting levels of IL-8 here.
Time Frame
at baseline and after 6 Months
Title
Plasma Cytokines - TNF-alpha
Description
Inflammatory and non-inflammatory cytokines levels will be tested in plasma at baseline and 6 months after intervention. We are reporting levels of TNF-alpha here.
Time Frame
at baseline and after 6 months
Title
Plasma Cytokines - IP-10
Description
Inflammatory and non-inflammatory cytokines levels will be tested in plasma at baseline and 6 months after intervention. We are reporting levels of IP-10 here.
Time Frame
at baseline and after 6 months
Title
Plasma Cytokines - MCP-4
Description
Inflammatory and non-inflammatory cytokines levels will be tested in plasma at baseline and 6 months after intervention. We are reporting levels of MCP-4 here.
Time Frame
at baseline and after 6 months
Title
Plasma Cytokines - MIP1-alpha
Description
Inflammatory and non-inflammatory cytokines levels will be tested in plasma at baseline and 6 months after intervention. We are reporting levels of MIP1-alpha here.
Time Frame
at baseline and after 6 months
Title
Plasma Cytokines - MIP1-beta
Description
Inflammatory and non-inflammatory cytokines levels will be tested in plasma at baseline and 6 months after intervention. We are reporting levels of MIP1-beta here.
Time Frame
at baseline and after 6 months
Title
Plasma Levels - Serotonin
Description
Plasma serotonin levels
Time Frame
at baseline and after 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: PD subjects will be adult men and women diagnosed with idiopathic mild to moderately severe PD defined as modified Hoehn & Yahr Stages I-III (while "On"). PD is defined according to the United Kingdom Brain Bank Criteria made at least six months prior to recruitment to the study. PD features include the presence of at least two of the four cardinal clinical manifestations of the disease, which are tremor, rigidity, bradykinesia, and disturbances of posture or gait, without any other known or suspected cause of Parkinsonism. Subjects should be stabilized on PD medication for at least 3 months before enrollment into the study. Subjects' PD drug prescriptions will not be altered nor withheld during the study, i.e., they will be tested while "On." The patient will have signed informed consent. Subjects who do not have PD (i.e., healthy or have other medical conditions such as traumatic brain injury (TBI), stroke, or other syndromes in which inflammation plays a role in the condition) will also be recruited as control subjects. This will allow us to estimate whether these other conditions show similar or unique inflammatory profile. Exclusion Criteria: Subjects will be excluded if they had previous brain surgery or other severe neurological problems intracerebral hemorrhage traumatic brain injury central nervous system malignancy active central nervous system (CNS) infection significant stroke Alzheimer disease or any type of implanted stimulator including but not limited to Deep Brain Stimulator (DBS) or pacemaker All subjects must be without evidence of dementia, defined as a score > 24 the Mini-Mental State Examination and able to understand test instructions Subjects must not have functional blindness (inability to participate in gait and visuomotor assessments) or lower limb amputation higher than the forefoot or any orthopedic problem that precludes performance of physical tests Allergic to niacin Significant cardiac, pulmonary, hepatic, gastrointestinal, or renal disease e.g., New York Heart Association Class III or IV congestive heart failure endocarditis pulmonary insufficiency symptomatic at rest or with mild physical exertion acute or chronic hepatitis renal failure requiring dialysis second and third degree atrioventricular block or sick sinus syndrome), or diabetes are also exclusionary factors
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chandramohan Wakade, MBBS
Organizational Affiliation
Charlie Norwood VA Medical Center, Augusta, GA
Official's Role
Principal Investigator
Facility Information:
Facility Name
Charlie Norwood VA Medical Center, Augusta, GA
City
Augusta
State/Province
Georgia
ZIP/Postal Code
30904
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
As the investigators request, we will share the data.
IPD Sharing Time Frame
One year after the study is closed.
IPD Sharing Access Criteria
When we are ready to publish, the data will be available.

Learn more about this trial

GPR109A and Parkinson's Disease: Role of Niacin in Outcome Measures

We'll reach out to this number within 24 hrs