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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00590408
Other study ID # 05-13642
Secondary ID 05-13642
Status Terminated
Phase Phase 4
First received December 28, 2007
Last updated November 27, 2009
Start date March 2006
Est. completion date August 2008

Study information

Verified date November 2009
Source Creighton University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Statins are medications that lower blood cholesterol by inhibiting cholesterol production in the liver. Overall, statins are well tolerated. Approximately 10% to 15% of patients report muscle aches/pain while taking statins. In a very small percentage of patients (<0.01%; less than one in 10,000 people), muscle aches/pains may be accompanied by more serious muscle damage. In these patients, statins must be discontinued. In some reports, patients taking statins have reduced blood levels of coenzyme Q10. Coenzyme Q10 is an essential protein which is present in all human cells needed for normal cell function. Coenzyme Q10 has been tested in patients with heart failure where it has been shown to be safe and effective. Many patients with heart conditions take coenzyme Q10, but the risks and benefits of supplementation with this product is unknown. Coenzyme Q10 is considered a dietary supplement and is not approved by the Food and Drug Administration (FDA) for any medical condition. Coenzyme Q10 has very few, if any, side effects. Upset stomach (gastritis), headache, body ache, and low blood pressure have been reported. The objectives of this project are to test the efficacy and safety of coenzyme Q10 in treating muscle aches/pain in patients already taking statins who develop these symptoms.


Recruitment information / eligibility

Status Terminated
Enrollment 10
Est. completion date August 2008
Est. primary completion date August 2008
Accepts healthy volunteers No
Gender Both
Age group 19 Years to 79 Years
Eligibility Inclusion Criteria:

- Patients who are taking statins and develop unexplained, persistent myalgia with a normal plasma creatinine kinase level

Exclusion Criteria:

- Women of childbearing potential

- Patients currently taking coenzyme Q10 (or have taken in the previous 30 days)

- Patients receiving concomitant niacin, fibric acid derivatives, bile acid sequestrants, or other drugs that effect cholesterol levels or interact with statins

- Patients with a history of alcoholism or malnutrition

- Patients who have had acute coronary syndrome or muscle trauma in the prior 7 days

- Patients with a history of chronic muscle/joint pain, fibromyalgia, or degenerative disk disease.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
coenzyme Q10
60mg capsule twice daily for 12 weeks
matching placebo
matching placebo capsule twice daily for 12 weeks

Locations

Country Name City State
United States The Cardiac Center of Creighton University Medical Center Omaha Nebraska

Sponsors (1)

Lead Sponsor Collaborator
Creighton University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary evaluate the efficacy coenzyme Q10 in the treatment of myalgia in patients receiving statin therapy every 3-5 days during the first week 2 weeks, then at 4 weeks and 12 weeks Yes
Secondary evaluate the safety of coenzyme Q10 in the treatment of myalgia in patients receiving statin therapy every 3-5 days during the first week 2 weeks, then at 4 week and 12 weeks Yes