Healia Clinical Trials Information Database

The Effect of Statins on Skeletal Muscle Function

Statins are a group of medications that are used to lower cholesterol levels. Although serious side effects are rare, some people taking statins experience muscle pain or weakness. This study will evaluate the number of people who experience mild muscle complaints and will determine the effect of statins on skeletal muscle strength, endurance, and aerobic exercise performance.

Description

Statins are the most effective medications for reducing high cholesterol levels. They are extremely well tolerated by the majority of people but can produce a variety of muscle-related side effects in some people. Of these side effects, the most serious is rhabdomyolysis, which involves muscle fiber damage that can begin as muscle pain and progress to a loss of muscle cells, kidney failure, and death. While rhabdomyolysis is extremely rare, some people experience the more common muscle-related side effects of statins, such as muscle pain (known as “myalgia”), cramps, and weakness. These more common side effects warrant attention because they may limit the use of statins, affect mobility, and increase the risk of injury in older individuals. Also, the term “muscle weakness,” often used by patients and their doctors, is not well defined and can refer to a wide range of complaints from simple fatigue to an actual inability to perform activities of daily living. It is important to describe and quantify in more detail the muscle-related side effects associated with statins. The purpose of this study is to determine the incidence of statin-induced mild muscle complaints and to determine the effect of statins on skeletal muscle strength, endurance, and aerobic exercise performance.

This study will enroll healthy people who have never received statin medications. First, participants will attend three study visits over a period of 2 weeks. These study visits will include blood collection, questionnaires on physical activity and pain, vital sign measurements, and body measurements, including height, weight, and head circumference. Participants will also complete two cardiopulmonary exercise stress tests on a treadmill and will undergo arm and leg strength testing. Some participants may undergo a muscle biopsy. Participants will then be randomly assigned to receive either 80 mg of atorvastatin or placebo on a daily basis for 6 months. Blood will be collected again at Month 3. At Month 6, participants will attend two study visits for repeat baseline measurements. All participants will be contacted by phone every other week during the 6-month treatment period to monitor adverse events and medication compliance.

Status: Recruiting (N/A). Started on January 1st, 2008.

Enrollment: 440 subjects

Study Type: Interventional

Study Design:

  • Allocation: Randomized
  • Intervention Model: Parallel Assignment
  • Masking: Double Blind (Subject
  • Investigator)

Conditions:

Interventions:

  • Drug: Atorvastatin (Lipitor)
  • Drug: Placebo

Eligibility

Inclusion Criteria:

  • Statin-naive (i.e., has never taken statins before)

Exclusion Criteria:

  • Previous use of statins

  • Current treatment with cholesterol- or triglyceride-lowering drugs

  • Impaired liver or kidney function

  • Untreated hypothyroidism or hyperthyroidism

  • Treatment with other medications known to increase risk of myopathy in atorvastatin-treated patients (e.g., cyclosporine, azithromycin, erythromycin, azole antifungals, fusidic acid)

  • Existing infection requiring treatment with antibiotic therapy

  • Consumption of greater that 1 quart of grapefruit juice per day

  • Documented history of neuroleptic malignant syndrome

  • Inherited muscle disorders or myopathy

  • Known sickle cell trait

  • Cancer within the 5 years prior to study entry

  • Diabetes

  • Currently being treated for high blood pressure

  • Coronary artery disease

  • Peripheral vascular disease

  • Physical disability or previous injury that prevents safe exercise testing

  • Pregnant or breastfeeding

Gender

Both

Mininum Age

20 Years

Maximum Age

N/A

Healthy Volunteers

Accepts Healthy Volunteers


Resources

Source: National Heart, Lung, and Blood Institute (NHLBI)

Authority: United States: Federal Government

Locations

  • Hartford Hospital
    Hartford
    Connecticut
    06102
    United States
  • University of Connecticut
    Storrs
    Connecticut
    06269
    United States
  • University of Massachusetts
    Amherst
    Massachusetts
    01003
    United States

Officials

  • Paul D. Thompson, MD (Principal Investigator, Hartford Hospital)

Sponsors

  • National Heart, Lung, and Blood Institute (NHLBI) (Lead Sponsor)

References

None.

Links

None.


Date Verified
April 1st, 2010
First Received
April 7th, 2010
Last Changed
April 7th, 2010

Information obtained from ClinicalTrials.gov on June 09, 2011. Link to the current ClinicalTrials.gov record.


All data in the Healia Clinical Trials Information Database and content displayed by the Healia Clinical Trials Search Engine are licensed from the National Institutes of Health (National Library of Medicine), which collects and maintains the data.

The Healia Clinical Trials Search Engine searches the data set at clinicaltrials.gov, providing up-to-date information about current clinical trials. In the Healia Clinical Trials Database you can find information on new experimental drugs, medical devices, and other types of treatments for all types of diseases. Each clinical trial description includes information about the phase of the trial (phase I, phase II, or phase III), the trial’s methods, such as whether it is a randomized, placebo controlled, double blind study, and the status of the trial including whether or not the trial is currently enrolling new participants.


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