Effect of Atorvastatin (Lipitor) on Gene Expression in People With Vascular Disease
NCT00293748 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 200
Last updated 2017-07-02
Summary
This study will determine if the drug Atorvastatin (Lipitor) changes the genetic material found in blood cells of people with vascular (blood vessel) disease. Vascular diseases affect the blood flow in the body and can lead to a heart attack or stroke. Information gained from this study could be used to develop a more reliable blood test that predicts the risk of heart attack or stroke.
People 21 and older who have two or more risk factors for developing vascular disease are eligible for this study. Candidates are screened with a medical history, physical examination, electrocardiogram, ultrasound of the carotid (neck) arteries, blood tests, and check of blood pressure and heart rate.
Participants are randomly assigned to one of four treatment groups. Three groups receive Lipitor in a dose of either 10, 20 or 40 milligrams; the fourth group receives a placebo. All take the study drug for 3 months. In addition, they undergo the following tests and procedures:
Study Phase I (Months 2-4)
Participants in all groups are seen once a month at the NIH Clinical Center for blood tests and monitoring of drug side effects.
Study Phase 2 (Months 5-10)
* Placebo group: Participants are given 40 mg of Lipitor for 3 months (months 5-7) and seen by a physician once a month during that time. Blood is drawn at the 7-month visit and then participants are referred back to their physicians. During months 8, 9 and 10, participants are called once a month to check on their health. Participation ends after the tenth month.
* Lipitor group: Participants are referred back to their physicians for months 5 and 6 and are called once a month. During month 7, they return to the clinic for a follow-up evaluation and blood test. Participation ends after the seventh month.
Conditions
- Vascular Disease
- Vascular Disease Risk
Sponsors & Collaborators
-
National Institute of Neurological Disorders and Stroke (NINDS)
lead NIH
Eligibility
- Min Age
- 21 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2006-02-13
- Completion
- 2008-12-15
Countries
- United States
Study Locations
More Related Trials
-
Systemic Immunomodulatory Effects and Pharmacogenetics of Atorvastatin in Early Atherosclerosis
NCT00361283 ·Status: COMPLETED ·Phase: PHASE4
-
Effect of Genetic Variation on Efficacy and Safety of Lipid-Lowering Drugs
NCT07008794 ·Status: COMPLETED
-
A Study Of Pharmacokinetics, Pharmacodynamics And Safety Of Adding ETC-1002 To Atorvastatin 80 mg
NCT02659397 ·Status: COMPLETED ·Phase: PHASE2
-
Statins for the Treatment of NASH
NCT04679376 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
A Study Examining Torcetrapib/Atorvastatin And Atorvastatin Effects On Clinical CV Events In Patients With Heart Disease
NCT00134264 ·Status: TERMINATED ·Phase: PHASE3
-
Effect of CYP3A Genetic Polymorphisms on the Pharmacokinetics of Atorvastatin
NCT00973986 ·Status: COMPLETED ·Phase: PHASE1
-
Drug Interaction Study - Assess Pharmacokinetics of Both AZD5672 and Atorvastatin
NCT00722956 ·Status: COMPLETED ·Phase: PHASE1
-
The Effect of MK0859 on Lipoprotein Metabolism in Patients With Dyslipidemia (0859-026 AM3)
NCT00990808 ·Status: COMPLETED ·Phase: PHASE1
-
LY2189265 and Atorvastatin Interaction Study
NCT01250834 ·Status: COMPLETED ·Phase: PHASE1
-
Effect of a Fibrate and a Statin on Endothelial Dysfunction
NCT00491400 ·Status: TERMINATED ·Phase: NA
-
Dose-ranging Efficacy and Pharmacokinetics Study of Intravenous Atorvastatin in Hypercholesterolemic Patients
NCT03611010 ·Status: COMPLETED ·Phase: PHASE2
-
A Study in People With High Cholesterol
NCT00133380 ·Status: COMPLETED ·Phase: PHASE2
-
A Study of LY3478045 in Healthy Participants
NCT04270370 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Evaluate LY3202328 in Overweight Healthy Participants and Dyslipidemia
NCT02714569 ·Status: COMPLETED ·Phase: PHASE1
-
Atorvastatin Therapy for the Prevention of Atrial Fibrillation (SToP-AF)
NCT00252967 ·Status: TERMINATED ·Phase: PHASE3
-
Bioavailability Study for New Atorvastatin Formulation
NCT00844376 ·Status: COMPLETED ·Phase: PHASE4
-
A Study of LY3502970 in Healthy Participants
NCT03929744 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Investigate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Administering Multiple Oral Doses of GSK1292263 Alone and With Atorvastatin
NCT01218204 ·Status: COMPLETED ·Phase: PHASE2
-
Drug-Drug Interaction Study Between Colchicine and Atorvastatin
NCT00960323 ·Status: COMPLETED ·Phase: PHASE1
-
Pharmacokinetics of Rosuvastatin and Atorvastatin in Pediatric Dyslipidemia Patients
NCT02364258 ·Status: COMPLETED ·Phase: PHASE1
-
Can Atorvastatin Improve Vascular Function in Women With a History of Preeclampsia?
NCT01278459 ·Status: COMPLETED ·Phase: PHASE3
-
Drug Interaction Study of ASC42 With Atorvastatin
NCT05464628 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of the Safety, Pharmacokinetic Drug Interaction and Efficacy of ETC-1002 and Atorvastatin in Subjects With Hypercholesterolemia
NCT01779453 ·Status: COMPLETED ·Phase: PHASE2
-
CARDS Is Designed To Show If Lowering Cholesterol With Atorvastatin In Type 2 Diabetics Without CV Disease Reduces The Risk Of CV Events
NCT00327418 ·Status: COMPLETED ·Phase: PHASE4
-
Genetic Influence on Statin Pharmacodynamics
NCT01569854 ·Status: WITHDRAWN