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Sponsored by: |
Bader, Ted, M.D. |
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Information provided by: | Bader, Ted, M.D. |
ClinicalTrials.gov Identifier: | NCT00446940 |
Different Doses of rosuvastatin and atorvastatin will be used to see if HCV viral load changes and liver tests change.
Condition | Intervention | Phase |
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Hepatitis C |
Drug: rosuvastatin Drug: atorvastatin |
Phase II |
Study Type: | Interventional |
Study Design: | Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study |
Official Title: | Dose Finding Trial of Rosuvastatin and Atorvastatin Versus Hepatitis C |
Ages Eligible for Study: | 18 Years to 75 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
United States, Oklahoma | |
VA Hospital | |
OKlahoma City, Oklahoma, United States, 73104 |
Principal Investigator: | Ted Bader, MD | VA Medical Center, Oklahoma City, OK |
Study ID Numbers: | 13133 |
Study First Received: | March 11, 2007 |
Last Updated: | September 8, 2008 |
ClinicalTrials.gov Identifier: | NCT00446940 |
Health Authority: | United States: Food and Drug Administration |
Virus Diseases Hepatitis Signs and Symptoms Liver Diseases Rosuvastatin |
Digestive System Diseases Hepatitis, Viral, Human Hepatitis C Atorvastatin |
Antimetabolites RNA Virus Infections Molecular Mechanisms of Pharmacological Action Flaviviridae Infections Therapeutic Uses |
Antilipemic Agents Enzyme Inhibitors Anticholesteremic Agents Hydroxymethylglutaryl-CoA Reductase Inhibitors Pharmacologic Actions |