HOME  | CONTACT  | PATIENT LOGIN  | CLINIC LOGIN  | FAQ
  • PATIENTS &
    HEALTHY VOLUNTEERS
  • INVESTIGATORS
  • CROS / SPONSORS
  • CAREERS
  • TRIAL ALERTS

TRIALS SEARCH
      
  • HEALTH NEWS

  • RSS FEEDS

  • ABOUT TRIALS

  • LINK TO US


View Clinical Trial (Medical Research Study)


Prospective Randomized Placebo-Controlled Trial of SimvaSTATin in the Prevention of COPD Exacerbations (STATCOPE)

Signup
Browse Studies

City:   San Francisco
State:   California
Zip Code:   94143
Conditions:   Pulmonary Disease, Chronic Obstructive
Purpose:   To determine the effect of daily administration of 40 mgms simvastatin taken for at least 12 months (range 12-36 months) on the frequency of exacerbations of chronic obstructive lung disease (COPD) in patients with moderate to severe COPD who are prone to exacerbations and do not have other indications for statin treatment.
Study Summary:   COPD exacerbation is a common complication that significantly contributes to the high morbidity, mortality and costs associated with COPD. COPD exacerbations are associated with heightened lung inflammation that may have systemic implications (e.g., peripheral muscle weakness, cognitive impairment, depression, stroke, acute coronary syndrome, and atherosclerosis). Statins are potent agents that significantly reduce vascular events in patients with increased risks due to prior cardiac or cerebral vascular events and elevated lipid profiles. Statins have pleiotropic effects that extend well beyond their lipid lowering effects and may be potent anti-inflammatory agents. Retrospective data conducted in COPD patients indicate that statin use is associated with markedly decreased rates of COPD hospitalization and stabilization of lung function. Decreases in mortality in COPD due to complications of flu-like illnesses and deaths due to cardiovascular events have also been reported. Inflammatory biomarkers (C-reactive protein and interleukin- 6) are reported to be elevated in moderate to severe COPD patients who are prone to exacerbations. Inflammatory biomarkers (C-reactive protein and interleukin- 6) are reported to be reduced by statin therapy in patients with hyperlipidemia and cardiovascular diseases. Treatments that can effectively lessen the prevalence and severity of COPD exacerbations are desperately needed
Criteria:   Inclusion Criteria: 1. Male and female subjects, 40-80 years of age. 2. Clinical diagnosis of at least moderate COPD as defined by the GOLD criteria: 1. Postbronchodilator FEV1/FVC < 70%, 2. Postbronchodilator FEV1 < 80% predicted, with or without chronic symptoms (i.e., cough, sputum production). 3. Cigarette consumption of 10 pack-years or more. Patients may or may not be active smokers. 4. Must meet one or more of the following 4 conditions 1. Be using supplemental O2 2. Receiving a course of systemic corticosteroids and/or antibiotics for respiratory problems in the past year, 3. Visiting an Emergency Department for a COPD exacerbation within the past year, or 4. Being hospitalized for a COPD exacerbation within the past year 5. Willingness to make return visits and availability by telephone for duration of study. 6. Free of active coronary disease 7. Subject with expected life expectancy > 36 months Exclusion Criteria: 1. Patients who: 1. are on statin drugs. 2. should be on statins based on established risk stratification. (Using the ATP-III risk calculator created by the DCC to determine 10 year risk). 2. Documented history of active CHD, such as unstable angina, prior myocardial infarction, stroke, symptomatic peripheral vascular or carotid artery disease, or congestive heart failure within the past 3 months. 3. A diagnosis of asthma. 4. The presence of a diagnosis other than COPD that results in the patient being either medically unstable, or having a predicted life expectancy < 3 years. 5. Special patient groups: prisoners, pregnant women, institutionalized patients 6. Women who are at risk of becoming pregnant during the study (pre-menopausal) and who refuse to use acceptable birth control (hormone-based oral or barrier contraceptive) for the duration of the study. 7. Woman using estradiol compounds for contraception. Postmenopausal women on estradiol compounds for hormone replacement therapy will be allowed into the trial. 8. Participants otherwise meeting the inclusion criteria will not be enrolled until they are a minimum of four weeks from their most recent acute exacerbation. 9. A clinical diagnosis of bronchiectasis defined as production of > one-half cup of purulent sputum/day. 10. Participants using niacin, azole antifungals (itraconazole, ketoconazole, posaconazole), fibric acid derivatives, erythromycin, clarithromycin, telithromycin, diltiazem, amlodipine , ranolazine,HIV protease inhibitors (such as indinavir), amiodarone, gemfibrozil, cyclosporine, verapamil, danazol, nefazodone, and red yeast rice extracts are excluded 11. Active liver disease. Active liver disease is defined as ALT, AST as greater than 1.5 times the upper limit of normal. 12. Patients with renal failure defined by serum creatinine greater than 3mg/dl. 13. Alcoholism. Alcoholism is defined as > 35 drinks per week. A drink is defined as one bottle of beer, one 8-ounce glass of wine, or one ounce of hard liquor. 14. Hypersensitivity to HMG CoA reductase inhibitors. Hypersensitivity is defined as an allergic reaction to statin, prior history of myopathy, rhabdomyolysis or previous intolerance to statin use. 15. Participants drinking greater than 4 cups (1qt) of grapefruit juice per day. 16. Participants drinking greater than 3 cups of green tea per day. 17. Diabetics will be excluded. Diabetics are defined by: 1. A CURRENT physician diagnosis of diabetes OR 2. CURRENT use of diabetic meds OR 3. Elevated HbA1c > 6.5% 18. The discretion of the Principal Investigator that the potential participant will not be a reliable study subject to complete the study requirements.
NCT ID:   NCT01061671
Primary Contact:   Principal Investigator
John E Connett, PhD
University of Minnesota (Data Coordinating Center)

Backup Contact:   N/A
Location Contact:   San Francisco, California 94143
United States

Rie Sakurai
Phone: 415-476-3259
Email: rie.sakurai@ucsf.edu

Site Status: Recruiting

Data Source:   ClinicalTrials.gov
Date Processed:   June 18, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
Click to view Full Listing


If you would like to be contacted by the clinical trial representative please enter your contact information, then click "I Am Interested In This Study"
First Name:  
Last Name:  
Email Address:  
Confirm Email:    
Daytime Phone (eg. 555-555-5555):  
City:  
State:
Zip Code:    
Best Time to Call:  
Questions/Comments:  
  • NEARBY STUDIES

Within 25 Miles

Early Alzheimer's Disease - San Francisco CA

Alzheimer's Disease - San Francisco CA

Teen Migraine Headaches - San Francisco CA

Postherpetic Neuralgia (Post-shingles pain) - San Francisco CA

Type 1 Diabetes - Walnut Creek CA

Healthy Volunteers (Ages 30-65) - Berkeley CA

Pediatric Migraines (Ages 12-17) - San Francisco CA

Within 50 Miles

Irritable Bowel Syndrome (IBS-D) - Sunnyvale CA

Postherpetic Neuralgia (Post-Shingles Pain) - Napa CA

Asthma (Ages 18-65) - San Jose CA

Low Back Pain and Constipation - Los Gatos CA

Uncontrolled Angina (Adult Stem Cell Research) - Stanford CA

Healthy Volunteers (Ages 50 -75) - Stanford CA

Obsessive-Compulsive Disorder - Stanford CA

Within 100 Miles

Asthma (Ages 18-65) - Roseville CA

Low Back Pain and Constipation - Roseville CA

Low Back Pain and Constipation - Sacramento CA

Low Back Pain and Constipation - Gold River CA

Chronic Sciatic Pain - Sacramento CA

Postherpetic Neuralgia (Post-Shingles Pain) - Sacramento CA

Arthritis - Sacramento CA

COPD (Emphysema and Chronic Bronchitis) - Sacramento CA

COPD (Emphysema and Chronic Bronchitis) - Sacramento CA

COPD (Emphysema and Chronic Bronchitis) - Roseville CA

COPD (Emphysema and Chronic Bronchitis)- Sacramento CA

Osteoartritis of the Hands - Roseville CA

Osteoartritis of the Hands - Sacramento CA

 
Clinical Connections Home | Investigators | CROs / Sponsors | Clinical Trials Notification | Search Clinical Trials | About Clinical Trials | Links | Terms And Conditions | Sitemap | Suggestions / Feedback
© 1998-2013 | All trademarks are property of their legal owners. | All Rights Reserved

ClinicalConnection.com is a resource that provides individuals with information regarding clinical trials that are being conducted worldwide.

ClinicalConnection.com does not conduct these clinical trials nor endorse them. Please consult your doctor or physician before participating.