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Preventing Central Catheter-Associated Bloodstream Infections

Primary Purpose

Catheter Infection, Catheter Infections Related

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Infection Prevention
Sponsored by
Abant Izzet Baysal University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Catheter Infection focused on measuring Catheter, Algorithms, Sepsis

Eligibility Criteria

18 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • A central venous catheter was inserted in the intensive care unit or before the intensive care unit admission, and being followed up in the intensive care unit with a central venous catheter.

Exclusion Criteria:

  • Patients whose central venous catheter was terminated during intensive care follow-up.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Central catheter-related bloodstream infection rates in intensive care units

    Arm Description

    Outcomes

    Primary Outcome Measures

    Infection rate
    Central catheter-related bloodstream infection rates in intensive care units

    Secondary Outcome Measures

    Full Information

    First Posted
    June 4, 2021
    Last Updated
    June 4, 2021
    Sponsor
    Abant Izzet Baysal University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04920877
    Brief Title
    Preventing Central Catheter-Associated Bloodstream Infections
    Official Title
    APPLICATION OF NURSE-FOCUSED ALGORITHM IN INTENSIVE CARE UNITS TO PREVENT CENTRAL CATHETER-RELATED BLOODSTREAM İNFECTİONS
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2021
    Overall Recruitment Status
    Unknown status
    Study Start Date
    June 4, 2021 (Anticipated)
    Primary Completion Date
    December 31, 2021 (Anticipated)
    Study Completion Date
    December 31, 2021 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Abant Izzet Baysal University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The research is an algorithm study focused on nursing care in order to prevent Central Catheter-Associated Bloodstream Infections in intensive care units. The algorithm prepared with infection control measures related to central catheter care will be applied with intensive care nurses and the effect of the algorithm on central catheter-related bloodstream infections will be examined. In practice, a 20-day preliminary assessment, a three-month intervention period, and a three-month post-intervention planning were made.
    Detailed Description
    In the light of literature review and guidelines, intensive care nurses will care for central catheters through an algorithm created with infection control measures. Nurse-focused algorithm content to prevent central catheter-related bloodstream infections Hand hygiene practice Use of personal protective equipment according to infection control measures Evaluation of the catheter insertion site in terms of redness, swelling, tenderness, discharge, bleeding Use of >0.5% chlorhexidine solution containing 70% alcohol for skin antisepsis at the catheter insertion site (if there is no chlorhexidine, povidone iodine + 70% alcohol solution is used) Changing the transparent, semi-permeable dressings every 5-7 days and gauze dressings every 48 hours for catheter dressing Catheter dressing with aseptic technique Use of sterile, preservative-free saline for flushing and locking in order to ensure the lumen of the catheter. Aseptic conditions should be observed if the junction of the catheter and the infusion set (Hub) is to be touched. Keeping the used triple taps closed Changing IV fluid sets and connection tools at appropriate times Daily assessment of CVC requirement The research will be carried out in the 1st, 2nd and 3rd Level Intensive Care Units of Bilecik Training and Research Hospital in Bilecik, Turkey. Infection rates will be compared in the study. In the study, the date of June 2021 will be taken as a preliminary assessment and training time for nurses. July-September 2021 will be the intervention period of the study, and October-December 2021 will be the post-intervention period.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Catheter Infection, Catheter Infections Related
    Keywords
    Catheter, Algorithms, Sepsis

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Model Description
    Patients followed with a central catheter in the intensive care unit
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    100 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Central catheter-related bloodstream infection rates in intensive care units
    Arm Type
    Experimental
    Intervention Type
    Other
    Intervention Name(s)
    Infection Prevention
    Intervention Description
    Preventing central catheter-related bloodstream infections in intensive care units
    Primary Outcome Measure Information:
    Title
    Infection rate
    Description
    Central catheter-related bloodstream infection rates in intensive care units
    Time Frame
    Three months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    100 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: A central venous catheter was inserted in the intensive care unit or before the intensive care unit admission, and being followed up in the intensive care unit with a central venous catheter. Exclusion Criteria: Patients whose central venous catheter was terminated during intensive care follow-up.

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Preventing Central Catheter-Associated Bloodstream Infections

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