Ubiquinol in Parkinson's Disease: Safety, Tolerability, and Effects Upon Oxidative Damage and Mitochondrial Biomarkers
Primary Purpose
Parkinson Disease
Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Ubiquinol
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Parkinson Disease focused on measuring Parkinson Disease, ubiquinol, CoQ10, magnetic resonance spectroscopy, lactate, glutathione
Eligibility Criteria
Inclusion Criteria:
- diagnosis of PD according to the Untied Kingdom (UK) Brain Bank Criteria, and confirmed by a Movement Disorders neurologist;
- age 40-75 years; diagnosis within 5 years of study participation;
- PD medications able to remain at stable doses in the opinion of the enrolling investigator;
- able to undergo MRI;
- absence of significant medical, psychiatric, and other neurological disease;
- absence of dementia and Mini-Mental State Examination (MMSE) > 26.
Exclusion Criteria:
- failure to meet diagnosis by above criteria;
- time since diagnosis > 5 years before study participation;
- PD medications not predicted to remain at stable doses in the opinion of the enrolling investigator;
- unable to undergo MRI;
- unable to comply with informed consent process;
- presence of significant medical, psychiatric (including major depressive disorder) or other neurological (including epilepsy, brain tumor, stroke) disease;
- diagnosis of dementia and/or MMSE 26 or lower;
- possibility of pregnancy (negative test required in women of childbearing age);
- taking medications including antipsychotic agents and dopamine- blocking anti-emetic agents;
- taking Coenzyme Q10;
- participation in another clinical trial within the last 3 months.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Ubiquinol
Placebo
Arm Description
600mg ubiquinol daily for 24 weeks
Placebo daily for 24 weeks
Outcomes
Primary Outcome Measures
Number of Adverse Events
The incidence and severity of adverse events in Parkinson disease patients taking 600mg ubiquinol or placebo daily over a 6 month period.
Secondary Outcome Measures
Cerebral Redox Markers
Change from baseline in lactate levels at 8 weeks as determined by Magnetic Resonance Spectroscopy
Full Information
NCT ID
NCT03061513
First Posted
February 13, 2017
Last Updated
April 24, 2017
Sponsor
Weill Medical College of Cornell University
1. Study Identification
Unique Protocol Identification Number
NCT03061513
Brief Title
Ubiquinol in Parkinson's Disease: Safety, Tolerability, and Effects Upon Oxidative Damage and Mitochondrial Biomarkers
Official Title
Ubiquinol in Parkinson's Disease: Safety, Tolerability, and Effects Upon Oxidative Damage and Mitochondrial Biomarkers
Study Type
Interventional
2. Study Status
Record Verification Date
April 2017
Overall Recruitment Status
Completed
Study Start Date
February 28, 2012 (Actual)
Primary Completion Date
December 31, 2016 (Actual)
Study Completion Date
December 31, 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Weill Medical College of Cornell University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to find out whether ubiquinol is well tolerated, can affect the symptoms of Parkinson's Disease and change the energy levels in the brain. Subjects will be randomized to taking ubiquinol or placebo and will have a neurological evaluation, magnetic resonance spectroscopy (MRS) and blood test for biological markers taken during the study.
Detailed Description
Multiple lines of evidence have implicated abnormal energy metabolism and deficient mitochondrial function in Parkinson's disease, presenting a unique target for therapy. A pilot study of ubiquinol in PD was therefore undertaken to determine its effects upon physiologic measures of mitochondrial metabolic function. The incorporation of a neuroimaging biomarker is particularly important, since changes would demonstrate our ability to achieve Central Nervous System (CNS) access from this an formulation, accompanied by a meaningful neurophysiologic effect. Hydrogen Proton Magnetic Resonance Spectroscopy Imaging (1H MRSI) is a technique that provides insight into the metabolism of several endogenous brain compounds, most notably N-acetyl-L-aspartate (NAA), choline-containing compounds (Cho), and creatine and phosphocreatine (Cr). A number of studies of mitochondrial function have now firmly established the utility of 1H MRSI in probing potential mitochondrial energy metabolism dysfunction, in primary mitochondrial disorders, but also in PD. This pilot study is therefore designed to test whether oral ubiquinol affects cerebral indices of mitochondrial dysfunction, as measured by 1H MRSI in patients with Parkinson's disease, and to gather preliminary information on the safety and tolerability of ubiquinol in individuals with PD.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson Disease
Keywords
Parkinson Disease, ubiquinol, CoQ10, magnetic resonance spectroscopy, lactate, glutathione
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
11 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Ubiquinol
Arm Type
Active Comparator
Arm Description
600mg ubiquinol daily for 24 weeks
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo daily for 24 weeks
Intervention Type
Drug
Intervention Name(s)
Ubiquinol
Intervention Description
Ubiquinol caplets 600mg/day
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
placebo
Primary Outcome Measure Information:
Title
Number of Adverse Events
Description
The incidence and severity of adverse events in Parkinson disease patients taking 600mg ubiquinol or placebo daily over a 6 month period.
Time Frame
at 24 weeks
Secondary Outcome Measure Information:
Title
Cerebral Redox Markers
Description
Change from baseline in lactate levels at 8 weeks as determined by Magnetic Resonance Spectroscopy
Time Frame
at baseline and 8 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
diagnosis of PD according to the Untied Kingdom (UK) Brain Bank Criteria, and confirmed by a Movement Disorders neurologist;
age 40-75 years; diagnosis within 5 years of study participation;
PD medications able to remain at stable doses in the opinion of the enrolling investigator;
able to undergo MRI;
absence of significant medical, psychiatric, and other neurological disease;
absence of dementia and Mini-Mental State Examination (MMSE) > 26.
Exclusion Criteria:
failure to meet diagnosis by above criteria;
time since diagnosis > 5 years before study participation;
PD medications not predicted to remain at stable doses in the opinion of the enrolling investigator;
unable to undergo MRI;
unable to comply with informed consent process;
presence of significant medical, psychiatric (including major depressive disorder) or other neurological (including epilepsy, brain tumor, stroke) disease;
diagnosis of dementia and/or MMSE 26 or lower;
possibility of pregnancy (negative test required in women of childbearing age);
taking medications including antipsychotic agents and dopamine- blocking anti-emetic agents;
taking Coenzyme Q10;
participation in another clinical trial within the last 3 months.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Claire Henchcliffe, MD DPhil
Organizational Affiliation
Weill Medical College of Cornell University
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Ubiquinol in Parkinson's Disease: Safety, Tolerability, and Effects Upon Oxidative Damage and Mitochondrial Biomarkers
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