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Sponsors and Collaborators: |
Yale University Washington Mutual Foundation |
Information provided by: | Yale University |
ClinicalTrials.gov Identifier: | NCT00259662 |
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.
Condition | Intervention |
Gynecologic Oncological Pelvic/Abdominal Surgery |
Drug: atorvastatin |
ChemIDplus related topics: | Atorvastatin Atorvastatin calcium |
Study Type: | Interventional |
Study Design: | Randomized, Double-Blind, Placebo Control, Parallel Assignment |
Official Title: | High-Dose Statin Therapy in the Perioperative Period and DVT Prevention. |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Female |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Ala S Haddadin, MD | 203-785-2802 | ala.haddadin@yale.edu |
Contact: Jessica L Feinleib, MD/Phd |
United States, Connecticut | |||||
Yale-New Haven Hospital | Recruiting | ||||
New Haven, Connecticut, United States, 06510 | |||||
Contact: Ala S Haddadin, MD 203-785-2802 ala.haddadin@yale.edu | |||||
Principal Investigator: Ala S Haddadin, MD |
Yale University |
Washington Mutual Foundation |
Principal Investigator: | Ala S Haddadin, MD | Assistant Professor |
Study ID Numbers: | HIC0507000393 |
First Received: | November 28, 2005 |
Last Updated: | November 30, 2005 |
ClinicalTrials.gov Identifier: | NCT00259662 |
Health Authority: | United States: Food and Drug Administration |
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