Clinical trial

7T Magnetic Resonance Spectroscopy and Skeletal Muscle Biopsy Findings in Statin

Name
STU 072016-015
Description
Over 40 million Americans take statins to reduce their risk of atherosclerotic cardiovascular disease (ASCVD). Unfortunately, 10 to 20% stop taking them due to statin-associated muscle symptoms (e.g. pain, aches, weakness, cramps, or stiffness) (1, 2). The pathophysiology of these statin-associated muscle symptoms (SAMS) has remained elusive. Consequently, no objective diagnostic method exists, causing confusion for patient and providers since muscle symptoms can often be multifactorial.
Trial arms
Trial start
2018-08-17
Estimated PCD
2021-12-20
Trial end
2021-12-20
Status
Terminated
Phase
Early phase I
Treatment
Simvastatin 40mg
40mg oral daily for 10 weeks
Arms:
Placebo, Simvastatin 40mg
Size
3
Primary endpoint
The Mitochondrial Changes In Muscles During Statin Use
10 weeks
Eligibility criteria
Inclusion • Adults, age \> 18 ys or \< 80 yrs. Patients reporting complaints of statin-associated muscle symptoms, aches, weakness, cramps, or stiffness in the legs. Exclusion Criteria * Patient who drink large quantities of grapefruit juice (\> 1 quart daily). * Patients on the following drugs for which the FDA has issued restrictions for using simvastatin 40 mg daily do to an increased risk of severe muscle injury such as itraconazole, posaconazole, ketoconazole, erythromycin, clarithromycin, telithromycin, HIV-1 protease inhibitors, nefazodone, gemfibrozil, cyclosporine, danazol, amiodarone, amlodipine, ranolazine, and verapamil. * Patients with muscle-related pain that is not related to statin-use (e.g. muscle aches from strain or trauma) or remains unexplained. * Any patients with underlying non-statin related muscle disorders. * Presence of any clinically significant uncontrolled endocrine disease known to influence serum lipids or lipoproteins. * Conditions of severe acute vascular stress (acute coronary syndrome, ischemic stroke, or major vascular surgery) within prior 3 months. * Any patients with a history of severe or life-threatening reactions to statins including rhabdomyolysis (defined as evidence of organ damage with CK \>10,000 IU/L), CK elevation \> 10 times the upper limit of normal, cognitive decline, transaminitis, or allergic reactions. * History of fibromyalgia or rheumatologic disease with symptoms that may be confounded with statin-related muscle complaints. * Patients unable to maintain their current activity level or planning to increase their activity level (e.g. new exercise regimen). Such changes may have acute effects on muscle metabolism. * Pregnant or breast-feeding women. Statins are teratogenic, and the effects of high magnetic fields on a fetus are unknown. * Women of reproductive age not on effective contraception. Adequate contraceptive measures include intrauterine device (IUD); bilateral tubal ligation; condom or diaphragm plus either contraceptive sponge, foam or jelly. * Any person with implanted metal, because of MRS safety. * Use of any active investigational drugs within 1 month or 5 half-lives, whichever is longer. * History of antibodies to HMGCoA.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE4'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'SINGLE_GROUP', 'primaryPurpose': 'BASIC_SCIENCE', 'maskingInfo': {'masking': 'TRIPLE', 'maskingDescription': 'Double Blind', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR']}}, 'enrollmentInfo': {'count': 3, 'type': 'ACTUAL'}}
Updated at
2023-02-14

1 organization

1 product

5 indications

Indication
Muscle Cramp
Indication
Ache
Indication
Weakness
Indication
Muscle