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Safety and Tolerability of Coenzyme Q10 in Hemodialysis Patients

Safety, Tolerability and Efficacy of Coenzyme Q10 in Hemodialysis Patients: Aim 1

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00908297
Enrollment
20
Registered
2009-05-25
Start date
2010-02-28
Completion date
2010-11-30
Last updated
2012-04-24

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

Conditions

Atherosclerosis, Cardiovascular Disease, End Stage Renal Disease, Oxidative Stress

Keywords

Cardiovascular disease, End stage renal disease, Atherosclerosis, Oxidative stress, Antioxidants

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.

Interventions

DIETARY_SUPPLEMENTCoenzyme Q10

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

Sponsors

National Center for Complementary and Integrative Health (NCCIH)
CollaboratorNIH
University of Washington
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Safety Measures: * Laboratory tests on serum: Comprehensive metabolic panel and creatinine phosphokinase. * Electrocardiogram, physical examination findings, and adverse events.Every two weeks
Efficacy Measures: Markers in the blood indicating oxidative stressEvery two weeks

Secondary

MeasureTime frame
Serum biomarkers of Cardiovascular condition and healthAt baseline study visit and last study visit

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 15, 2026