Trials / Completed
CompletedNCT00610545
Atorvastatin in Perioperative Vascular Surgery - Pilot Study
Atorvastatin 80mg Versus Atorvastatin 20mg in Perioperative Vascular Surgery to Evaluate Cardiovascular Outcomes
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 100 (estimated)
- Sponsor
- University of Campinas, Brazil · Academic / Other
- Sex
- All
- Age
- 40 Years – 90 Years
- Healthy volunteers
- Not accepted
Summary
This study is designed to determine if the use of atorvastatin (Lipitor), a member of the HMG coA reductase inhibitor class of drugs referred to as statins, will reduce cardiovascular outcomes ( mortality - myocardial infarction - stroke ) when given in high doses in comparative standard doses in the perioperative period of major vascular surgery. Abdominal aortic aneurysm , Carotid endarterectomy , Revascularization of lower limbs
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Atorvastatin | Atorvastatin 80 mg; Use Atorvastatin for 60 days , and the vascular surgery will be made between day-7 and day-60 |
| DRUG | Atorvastatin | Atorvastatin 20 mg; Use Atorvastatin for 60 days , and the vascular surgery will be made between day-7 and day-60 |
Timeline
- Start date
- 2007-07-01
- Primary completion
- 2008-09-01
- Completion
- 2008-12-01
- First posted
- 2008-02-08
- Last updated
- 2009-02-16
Locations
1 site across 1 country: Brazil
Source: ClinicalTrials.gov record NCT00610545. Inclusion in this directory is not an endorsement.