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Antibiotic Treatment for Infections of Short Term In-dwelling Vascular Catheters Due to Gram Positive Bacteria

Primary Purpose

Bacterial Infections, Gram-Positive Bacterial Infections, Bacteremia

Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Linezolid
Vancomycin
Oxacillin
Dicloxacillin
Sponsored by
Pfizer
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bacterial Infections

Eligibility Criteria

13 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients with a central indwelling catheter with signs and symptoms of infection Exclusion Criteria: Patients with tunneled catheter which cannot be removed. Patients with evidence of endovascular infection including endocarditis. Patients with infection of permanent intravascular devices. Patients who have received more than 1 day of another antibiotic before enrollment. Patients with HIV and low CD4 count.

Sites / Locations

    Outcomes

    Primary Outcome Measures

    The empiric treatment of patients with complicated skin and skin structure infections (cSSSI) related to an indwelling catheter;
    The empiric treatment of patients with gram-positive catheter-related bloodstream infections.

    Secondary Outcome Measures

    Clinical efficacy of linezolid compared to vancomycin/oxacillin/dicloxacillin.2.Incidence of late metastatic sequelae associated with S. aureus infections in patients treated with linezolid

    Full Information

    First Posted
    May 14, 2002
    Last Updated
    September 11, 2009
    Sponsor
    Pfizer
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00037050
    Brief Title
    Antibiotic Treatment for Infections of Short Term In-dwelling Vascular Catheters Due to Gram Positive Bacteria
    Official Title
    Linezolid vs. Vancomycin/Oxacillin/Dicloxacillin in the Treatment of Catheter-Related Gram-Positive Bloodstream Infections
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2009
    Overall Recruitment Status
    Completed
    Study Start Date
    April 2002 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    July 2005 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Pfizer

    4. Oversight

    5. Study Description

    Brief Summary
    This study will treat patients who have a short term central catheter that is thought to be infected with a specific bacteria (gram positive bacteria)

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Bacterial Infections, Gram-Positive Bacterial Infections, Bacteremia

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    739 (Actual)

    8. Arms, Groups, and Interventions

    Intervention Type
    Drug
    Intervention Name(s)
    Linezolid
    Other Intervention Name(s)
    Zyvox
    Intervention Type
    Drug
    Intervention Name(s)
    Vancomycin
    Intervention Type
    Drug
    Intervention Name(s)
    Oxacillin
    Intervention Type
    Drug
    Intervention Name(s)
    Dicloxacillin
    Primary Outcome Measure Information:
    Title
    The empiric treatment of patients with complicated skin and skin structure infections (cSSSI) related to an indwelling catheter;
    Title
    The empiric treatment of patients with gram-positive catheter-related bloodstream infections.
    Secondary Outcome Measure Information:
    Title
    Clinical efficacy of linezolid compared to vancomycin/oxacillin/dicloxacillin.2.Incidence of late metastatic sequelae associated with S. aureus infections in patients treated with linezolid

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    13 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients with a central indwelling catheter with signs and symptoms of infection Exclusion Criteria: Patients with tunneled catheter which cannot be removed. Patients with evidence of endovascular infection including endocarditis. Patients with infection of permanent intravascular devices. Patients who have received more than 1 day of another antibiotic before enrollment. Patients with HIV and low CD4 count.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Pfizer CT.gov Call Center
    Organizational Affiliation
    Pfizer
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Links:
    URL
    http://www.fda.gov/Drugs/DrugSafety/PostmarketDrugSafetyInformationforPatientsandProviders/ucm101503.htm
    Description
    Link to FDA Alert

    Learn more about this trial

    Antibiotic Treatment for Infections of Short Term In-dwelling Vascular Catheters Due to Gram Positive Bacteria

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