Safety and Efficacy Study of Angiotech Central Venous Catheter to Prevent Bacterial Catheter Colonization

Last updated: January 22, 2013
Sponsor: Angiotech Pharmaceuticals
Overall Status: Completed

Phase

3

Condition

Bacterial Infections

Treatment

N/A

Clinical Study ID

NCT00288418
011-ACVC05
  • Ages > 18
  • All Genders

Study Summary

The main purpose of this study is to determine if the Angiotech central venous catheter (CVC) is equal in effectiveness to a CVC coated with chlorhexidine and silver sulfadiazine in preventing bacterial catheter colonization. Other objectives of this study are to determine if the Angiotech CVC is equal in effectiveness to a CVC coated with chlorhexidine and silver sulfadiazine in preventing catheter-related local infection, and catheter-related bloodstream infection. This study will also assess the safety of the Angiotech CVC.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • at least 18 years of age

  • Be initially hospitalized in an intensive care setting

  • Require insertion of a triple-lumen central venous catheter for an anticipated periodof up to 28 days

  • If female and of child-bearing potential, provide evidence of a negative pregnancytest

Exclusion

Exclusion Criteria:

  • Has a life expectancy of less than one month

  • Is pregnant

  • Has a history of anaphylactic reactions, including reactions to contrast dyes

  • Has a history of allergy to 5-fluorouracil (5-FU) or chlorhexidine

Study Design

Total Participants: 960
Study Start date:
December 01, 2005
Estimated Completion Date:
July 31, 2007

Study Description

Central venous catheters are widely used for hemodynamic monitoring and the administration of fluids, drugs, and nutrition. The most frequent life-threatening complication of central venous catheter use is septicemia. Normal cutaneous flora may invade the intracutaneous tract during or after catheter insertion. The colonizing bacteria subsequently disseminate along the catheter surface and ultimately seed into the blood stream.

In the United States, a total of 250,000 cases of central venous catheter-related infections are estimated annually. Costs per infection are estimated as high as US$56,000. It is clinically imperative that effective measures be found to decrease catheter infection rates while minimizing the risk of the development of microbial resistance.

Primary Objective: The primary objective of this study is to determine the non-inferiority of the Angiotech Central Venous Catheter (CVC) when compared to the ARROWgard Blue® CVC to prevent bacterial catheter colonization.

Secondary Objectives: The secondary objectives of this study are to determine the non-inferiority of the Angiotech CVC when compared to the ARROWgard Blue® CVC to prevent:

  1. catheter-related local infection; and

  2. catheter-related bloodstream infection.

Safety Objectives: This study will assess the safety of the Angiotech CVC.

Connect with a study center

  • Cardio-Thoracic Surgeons, P.C.

    Birmingham, Alabama 35235
    United States

    Site Not Available

  • Pulmonary Consultant Group

    Orange, California 92868
    United States

    Site Not Available

  • Pulmonary Center Sharp Memorial Hospital

    San Diego, California 92123
    United States

    Site Not Available

  • Kaiser Permanente Santa Teresa

    San Jose, California 95119
    United States

    Site Not Available

  • Denver Health Medical Center

    Denver, Colorado 80204
    United States

    Site Not Available

  • Christiana Care Research Institute

    Newark, Delaware 19713
    United States

    Site Not Available

  • Florida Research Network, LLC

    Gainesville, Florida 32605
    United States

    Site Not Available

  • Atlanta Institute for Medical Research Inc

    Decatur, Georgia 30030
    United States

    Site Not Available

  • Kerry Thibodeaux, M.D.

    Opelousas, Louisiana 70570
    United States

    Site Not Available

  • UMASS Medical School, Dept of Anesthesiology

    Worcester, Massachusetts 01655
    United States

    Site Not Available

  • Newark Beth Israel Hospital

    Newark, New Jersey 07112
    United States

    Site Not Available

  • Pulmonary and Critical Care Medicine

    Cincinnati, Ohio 45267
    United States

    Site Not Available

  • Medical University of Ohio

    Toledo, Ohio 43614
    United States

    Site Not Available

  • St Vincent Mercy Medical Center, Bldg 1

    Toledo, Ohio 43608
    United States

    Site Not Available

  • Universty of Oklahoma HSC

    Oklahoma City, Oklahoma 73104
    United States

    Site Not Available

  • Drexel University College of Medicine

    Philadelphia, Pennsylvania 19102
    United States

    Site Not Available

  • Rhode Island Hospital

    Providence, Rhode Island 02903
    United States

    Site Not Available

  • Rapid City Regional Hospital

    Rapid City, South Dakota 57701
    United States

    Site Not Available

  • University of Virginia, Department of Anesthesiology

    Charlottesville, Virginia 22908
    United States

    Site Not Available

  • Winchester Medical Center

    Winchester, Virginia 22601
    United States

    Site Not Available

  • Franciscan Health System Research Center

    Tacoma, Washington 98405
    United States

    Site Not Available

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.