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High-Dose Periop Statins for Prevention of DVT

This study is currently recruiting participants.
Verified by Yale University, November 2005

Sponsors and Collaborators: Yale University
Washington Mutual Foundation
Information provided by: Yale University
ClinicalTrials.gov Identifier: NCT00259662
  Purpose

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   

U.S. FDA Resources

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.

Further study details as provided by Yale University:

Primary Outcome Measures:
  • Decrease in incidence of deep vein thrombosis

Secondary Outcome Measures:
  • Decrease in inflammatory mediator release.

Estimated Enrollment:   150
Study Start Date:   November 2005

  Eligibility
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

  • gynecologic tumor scheduled for resection

Exclusion Criteria:

  • prior reaction to statins
  • renal insufficiency
  • liver disease
  • h/o alcoholism
  • prior h/o DVT or hypercoagulability
  • concurrent medicatins that signicantly affect cytochrome P450 3A4
  • breast feeding or pregnancy
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00259662

Contacts
Contact: Ala S Haddadin, MD     203-785-2802     ala.haddadin@yale.edu    
Contact: Jessica L Feinleib, MD/Phd    

Locations
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            

Sponsors and Collaborators
Yale University
Washington Mutual Foundation

Investigators
Principal Investigator:     Ala S Haddadin, MD     Assistant Professor    
  More Information


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

Keywords provided by Yale University:
cancer--ovarian  
cancer--endometria  
deep vein thrombosis  
statin therapy in perioperative period  

Study placed in the following topic categories:
Venous Thrombosis
Atorvastatin
Thrombosis

Additional relevant MeSH terms:
Antimetabolites
Molecular Mechanisms of Pharmacological Action
Therapeutic Uses
Antilipemic Agents
Enzyme Inhibitors
Anticholesteremic Agents
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Pharmacologic Actions

ClinicalTrials.gov processed this record on October 06, 2008




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