Safety and Tolerability of Coenzyme Q10 in Hemodialysis Patients
Primary Purpose
Cardiovascular Disease, End Stage Renal Disease, Atherosclerosis
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Coenzyme Q10
Sponsored by
About this trial
This is an interventional prevention trial for Cardiovascular Disease focused on measuring Cardiovascular disease, End stage renal disease, Atherosclerosis, Oxidative stress, Antioxidants
Eligibility Criteria
Inclusion Criteria:
- Patients with end-stage renal disease receiving thrice weekly hemodialysis
- Age > 18 and < 85 years
- Life expectancy greater than one year
- Ability to understand and provide informed consent for participation in the study
- Mean baseline plasma F2-isoprostane concentration > 50 pg/mL
Exclusion Criteria:
- History of poor adherence to hemodialysis or medical regimen
- Prisoners, patients with significant mental illness, and other vulnerable populations
- AIDS (HIV seropositivity is not an exclusion criteria)
- Active malignancy excluding basal cell carcinoma of the skin
- Gastrointestinal dysfunction requiring parenteral nutrition
- History of functional kidney transplant < 6 months prior to study entry
- Anticipated live donor kidney transplant
- Patients taking vitamin E supplements > 60 IU/day, vitamin C > 50 mg/day or other antioxidant or nutritional supplements
- Incident hemodialysis patients (defined as within 90 days of dialysis initiation)
- Patients hospitalized within the past 60 days
- Patients being dialyzed with a tunneled catheter as a temporary vascular access
- Patients with a history of a major atherosclerotic event (defined as combined incidence of myocardial infarction, urgent target-vessel revascularization, coronary bypass surgery, and stroke) within six months
Sites / Locations
- Northwest Kidney Centers - Scribner
Outcomes
Primary Outcome Measures
Safety Measures: * Laboratory tests on serum: Comprehensive metabolic panel and creatinine phosphokinase. * Electrocardiogram, physical examination findings, and adverse events.
Efficacy Measures: Markers in the blood indicating "oxidative stress"
Secondary Outcome Measures
Serum biomarkers of Cardiovascular condition and health
Full Information
NCT ID
NCT00908297
First Posted
May 21, 2009
Last Updated
April 20, 2012
Sponsor
University of Washington
Collaborators
National Center for Complementary and Integrative Health (NCCIH)
1. Study Identification
Unique Protocol Identification Number
NCT00908297
Brief Title
Safety and Tolerability of Coenzyme Q10 in Hemodialysis Patients
Official Title
Safety, Tolerability and Efficacy of Coenzyme Q10 in Hemodialysis Patients: Aim 1
Study Type
Interventional
2. Study Status
Record Verification Date
April 2012
Overall Recruitment Status
Completed
Study Start Date
February 2010 (undefined)
Primary Completion Date
October 2010 (Actual)
Study Completion Date
November 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
National Center for Complementary and Integrative Health (NCCIH)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to determine the safety and tolerability of the dietary supplement Coenzyme Q10 in hemodialysis patients.
Detailed Description
There are more than 400,000 patients receiving dialysis in the United States, and we expect that this number will go up. For those on hemodialysis, cardiovascular disease (CVD) accounts for a large part of the health problems that these patients have. Cardiovascular problems come from damage to the heart or blood vessels.
At present, we have no treatments proven to help prevent CVD in those on dialysis. For the general population, we know about many factors that increase the risk of CVD, such as having a high level of "bad" cholesterol. But for people on dialysis, we believe that there are other risk factors that are just as important in the development of CVD.
People on dialysis often have high blood levels of waste products. This is called "uremia". We believe that uremia can set up chemical reactions in the blood which can lead to hardening of the arteries (atherosclerosis), an important part of CVD. Compounds called antioxidants, which stop the chemical reactions, may help prevent CVD.
Coenzyme Q10 is a naturally occurring compound in blood and tissues. It is also a readily available dietary supplement often used as an alternative and complementary medicine. It is a powerful antioxidant. Previous studies have shown that blood levels of coenzyme Q10 are decreased in hemodialysis patients. Because of this, it is important for us to find out if giving coenzyme Q10 to hemodialysis patients can help prevent CVD. However, at present, there are no studies which carefully look at the safety and tolerability of coenzyme Q10, and whether it helps stops the harmful chemical reactions in the blood.
In addition, many people take medications called "statins" to help reduce risk for cardiovascular disease. We know that statins can lower coenzyme Q10. It is important for us to know if hemodialysis patients taking statins have lower levels of coenzyme Q10. It may be that therapy with coenzyme Q10 could increase the beneficial effects of statin therapy in hemodialysis patients.
In this study, we will test to see if different doses of the dietary supplement coenzyme Q10 will be safe and well tolerated in hemodialysis patients. This is with a view to later studies to determine if coenzyme Q10 will help stop harmful chemical reactions in the blood for hemodialysis patients. This study will help us prepare for future studies of coenzyme Q10, by demonstrating the safely and tolerability of this compound in hemodialysis patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiovascular Disease, End Stage Renal Disease, Atherosclerosis, Oxidative Stress
Keywords
Cardiovascular disease, End stage renal disease, Atherosclerosis, Oxidative stress, Antioxidants
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Dietary Supplement
Intervention Name(s)
Coenzyme Q10
Other Intervention Name(s)
CoQ10
Intervention Description
By mouth (wafer) once daily for duration of study (8 weeks).
Dose escalation:
300 mg for two weeks
600 mg for two weeks
1200 mg for two weeks
1800 mg for final two weeks
Primary Outcome Measure Information:
Title
Safety Measures: * Laboratory tests on serum: Comprehensive metabolic panel and creatinine phosphokinase. * Electrocardiogram, physical examination findings, and adverse events.
Time Frame
Every two weeks
Title
Efficacy Measures: Markers in the blood indicating "oxidative stress"
Time Frame
Every two weeks
Secondary Outcome Measure Information:
Title
Serum biomarkers of Cardiovascular condition and health
Time Frame
At baseline study visit and last study visit
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with end-stage renal disease receiving thrice weekly hemodialysis
Age > 18 and < 85 years
Life expectancy greater than one year
Ability to understand and provide informed consent for participation in the study
Mean baseline plasma F2-isoprostane concentration > 50 pg/mL
Exclusion Criteria:
History of poor adherence to hemodialysis or medical regimen
Prisoners, patients with significant mental illness, and other vulnerable populations
AIDS (HIV seropositivity is not an exclusion criteria)
Active malignancy excluding basal cell carcinoma of the skin
Gastrointestinal dysfunction requiring parenteral nutrition
History of functional kidney transplant < 6 months prior to study entry
Anticipated live donor kidney transplant
Patients taking vitamin E supplements > 60 IU/day, vitamin C > 50 mg/day or other antioxidant or nutritional supplements
Incident hemodialysis patients (defined as within 90 days of dialysis initiation)
Patients hospitalized within the past 60 days
Patients being dialyzed with a tunneled catheter as a temporary vascular access
Patients with a history of a major atherosclerotic event (defined as combined incidence of myocardial infarction, urgent target-vessel revascularization, coronary bypass surgery, and stroke) within six months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jonathan Himmelfarb, MD
Organizational Affiliation
University of Washington - Kidney Research Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwest Kidney Centers - Scribner
City
Seattle
State/Province
Washington
ZIP/Postal Code
98122
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
26531095
Citation
Yeung CK, Billings FT 4th, Claessens AJ, Roshanravan B, Linke L, Sundell MB, Ahmad S, Shao B, Shen DD, Ikizler TA, Himmelfarb J. Coenzyme Q10 dose-escalation study in hemodialysis patients: safety, tolerability, and effect on oxidative stress. BMC Nephrol. 2015 Nov 3;16:183. doi: 10.1186/s12882-015-0178-2.
Results Reference
derived
Links:
URL
http://www.nwkidney.org/
Description
Northwest Kidney Centers
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Safety and Tolerability of Coenzyme Q10 in Hemodialysis Patients
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