Effectiveness of Creatine in Preventing Muscle Aching From Cholesterol-Lowering Statin Drugs
Primary Purpose
Hypercholesterolemia, Aches, Cramps
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Creatine
Sponsored by
About this trial
This is an interventional supportive care trial for Hypercholesterolemia focused on measuring Hydroxymethylglutaryl-CoA Reductase Inhibitors, Creatine, Adverse Effects, Muscle Toxicity
Eligibility Criteria
Inclusion Criteria:
- hypercholesterolemia in need of aggressive treatment, defined as a high risk of a vascular event, thus subjects with diabetes, pre-diabetes, or known vascular disease
- intolerance (i.e. muscle toxicity symptoms) of at least 3 statin drugs, each confirmed on rechallenge
Exclusion Criteria:
- history of elevated CPK or rhabdomyolysis while taking a statin,
- CPK levels elevated above the normal range at baseline,
- pregnancy.
- renal insufficiency, defined as a serum creatinine ≥ 2.0 mg/dl.
- history of congestive heart failure.
Sites / Locations
- Wooster Family Health Center, Cleveland Clinic
Outcomes
Primary Outcome Measures
Combined visual analog pain scales (0-10) for aching, cramping and weakness
Secondary Outcome Measures
Full Information
NCT ID
NCT00797407
First Posted
November 24, 2008
Last Updated
November 24, 2008
Sponsor
The Cleveland Clinic
1. Study Identification
Unique Protocol Identification Number
NCT00797407
Brief Title
Effectiveness of Creatine in Preventing Muscle Aching From Cholesterol-Lowering Statin Drugs
Official Title
Creatine Supplementation for the Prevention of Statin Myalgia
Study Type
Interventional
2. Study Status
Record Verification Date
November 2008
Overall Recruitment Status
Completed
Study Start Date
August 2006 (undefined)
Primary Completion Date
December 2006 (Actual)
Study Completion Date
December 2006 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
The Cleveland Clinic
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to determine of creatine will prevent or treat the muscle toxicity side effect of statin drug therapy, whose symptoms are aching, cramping, and weakness. This is tested in patients who have had this side effect from 3 different statin drugs.
Detailed Description
Muscle toxicity is the most common limiting side effect of statin therapy. Biochemical studies have suggested the presence of intramuscular creatine deficiency in patients with muscle toxicity. This is a test of oral creatine supplementation in statin intolerant subjects as a method of preventing the onset of this side effect as well as resolving these symptoms when present during statin therapy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypercholesterolemia, Aches, Cramps, Weakness
Keywords
Hydroxymethylglutaryl-CoA Reductase Inhibitors, Creatine, Adverse Effects, Muscle Toxicity
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Dietary Supplement
Intervention Name(s)
Creatine
Other Intervention Name(s)
creatine monohydrate
Intervention Description
Creatine 5 gm orally twice a day for 5 days, followed by 5 gm once a day
Primary Outcome Measure Information:
Title
Combined visual analog pain scales (0-10) for aching, cramping and weakness
Time Frame
baseline, after 5 days of creatine loading, after 6 weeks of creatine+statin, after up to 6 weeks on statin without creatine, after 4 days of rechallenge with creatine while still on statin
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
hypercholesterolemia in need of aggressive treatment, defined as a high risk of a vascular event, thus subjects with diabetes, pre-diabetes, or known vascular disease
intolerance (i.e. muscle toxicity symptoms) of at least 3 statin drugs, each confirmed on rechallenge
Exclusion Criteria:
history of elevated CPK or rhabdomyolysis while taking a statin,
CPK levels elevated above the normal range at baseline,
pregnancy.
renal insufficiency, defined as a serum creatinine ≥ 2.0 mg/dl.
history of congestive heart failure.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David A Shewmon, MD
Organizational Affiliation
The Cleveland Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Wooster Family Health Center, Cleveland Clinic
City
Wooster
State/Province
Ohio
ZIP/Postal Code
44691
Country
United States
12. IPD Sharing Statement
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Effectiveness of Creatine in Preventing Muscle Aching From Cholesterol-Lowering Statin Drugs
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