A Swiss Study With Atorvastatin in Hyperlipidemic Patients Measuring LDL-Cholesterol (ACTFAST SWISS)
This study has been completed.
Sponsor:
Pfizer
Information provided by:
Pfizer
ClinicalTrials.gov Identifier:
NCT00136942
First received: August 25, 2005
Last updated: February 28, 2008
Last verified: April 2007
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Purpose
The proportion of patients achieving LDL-C target as defined by Swiss cholesterol recommendations (AGLA-recommendations) across starting doses of 10 mg, 20 mg, 40 mg, and 80 mg of atorvastatin.
| Condition | Intervention | Phase |
|---|---|---|
|
Hyperlipidemia |
Drug: Atorvastatin |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A Multicenter, 6-Week-Treatment, Open-Label Study Assessing The Percentage Of Hyperlipidemic Patients Achieving Low Density Lipoprotein Cholesterol Target With Atorvastatin |
Resource links provided by NLM:
MedlinePlus related topics:
Cholesterol
Drug Information available for:
Atorvastatin calcium
U.S. FDA Resources
Further study details as provided by Pfizer:
Primary Outcome Measures:
- The proportion of patients achieving LDL-C target as defined by local swiss AGLArecommendations across starting doses of 10 mg, 20 mg, 40 mg, and 80 mg of atorvastatin.
Secondary Outcome Measures:
- The proportion of patients across different AGLA-categories (primary and secondary prevention) achieving LDL-C target as defined by AGLA-recommendations across starting doses of 10 mg, 20 mg, 40 mg, and 80 mg of atorvastatin.
| Estimated Enrollment: | 370 |
| Study Start Date: | April 2005 |
Eligibility| Ages Eligible for Study: | 18 Years to 80 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Risk factors and diagnosis of dyslipidemia according to the AGLA-recommendations (see appendix B) at screening
- LDL-C < 6.0 mmol/l
- Triglyceride level < 5.0 mmol/l.
Exclusion Criteria:
- Subjects receiving higher than "usual maintenance" doses of Lipid Lowering Therapy (LLT) at screening.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00136942
Locations
| Switzerland | |
| Pfizer Investigational Site | |
| Langenthal, BE, Switzerland | |
| Pfizer Investigational Site | |
| Thun, BE, Switzerland | |
| Pfizer Investigational Site | |
| Binningen, BL, Switzerland | |
| Pfizer Investigational Site | |
| Liestal, BL, Switzerland | |
| Pfizer Investigational Site | |
| Basel, BS, Switzerland | |
| Pfizer Investigational Site | |
| Duedingen, FR, Switzerland | |
| Pfizer Investigational Site | |
| Geneve, GE, Switzerland | |
| Pfizer Investigational Site | |
| Onex, GE, Switzerland | |
| Pfizer Investigational Site | |
| Pfaeffikon, SZ, Switzerland | |
| Pfizer Investigational Site | |
| Siebnen, SZ, Switzerland | |
| Pfizer Investigational Site | |
| Lugano, TI, Switzerland | |
| Pfizer Investigational Site | |
| Malvaglia, TI, Switzerland | |
| Pfizer Investigational Site | |
| Melide, TI, Switzerland | |
| Pfizer Investigational Site | |
| Vezia, TI, Switzerland | |
| Pfizer Investigational Site | |
| Ecublens, VD, Switzerland | |
| Pfizer Investigational Site | |
| Lausanne, VD, Switzerland | |
| Pfizer Investigational Site | |
| Prilly, VD, Switzerland | |
| Pfizer Investigational Site | |
| Unteraegeri, ZG, Switzerland | |
| Pfizer Investigational Site | |
| Zug, ZG, Switzerland | |
| Pfizer Investigational Site | |
| Zuerich, ZH, Switzerland | |
Sponsors and Collaborators
Pfizer
Investigators
| Study Director: | Pfizer CT.gov Call Center | Pfizer |
More Information
Additional Information:
No publications provided
| ClinicalTrials.gov Identifier: | NCT00136942 History of Changes |
| Other Study ID Numbers: | A2581089 |
| Study First Received: | August 25, 2005 |
| Last Updated: | February 28, 2008 |
| Health Authority: | Switzerland: Swissmedic |
Additional relevant MeSH terms:
|
Hyperlipidemias Dyslipidemias Lipid Metabolism Disorders Metabolic Diseases Atorvastatin Hydroxymethylglutaryl-CoA Reductase Inhibitors Anticholesteremic Agents |
Hypolipidemic Agents Antimetabolites Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Enzyme Inhibitors Lipid Regulating Agents Therapeutic Uses |
ClinicalTrials.gov processed this record on May 21, 2013