High-dose Periop Statins for Prevention of DVT
Completed · Not applicable
Conditions studied: Gynecologic Oncological Pelvic/Abdominal Surgery
In brief
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 inflammatory responses and deep vein thrombosis formation when given in high doses in the perioperative period.
Key facts
- Study ID
- NCT00259662
- Run by
- Yale University
- People needed
- 29
- Starts
- 2005-11-01
- Expected to finish
- 2007-08-01
- Last updated by the study team
- 2016-12-01
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- gynecologic tumor scheduled for resection
You may not qualify if…
- prior reaction to statins
- renal insufficiency
- liver disease
- h/o alcoholism
- prior h/o DVT or hypercoagulability
- concurrent medications that significantly affect cytochrome P450 3A4
- breast feeding or pregnancy
Where it is running
- Yale-New Haven Hospital — New Haven, Connecticut, United States
Full record on ClinicalTrials.gov
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