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
About this trial
This is an interventional prevention trial for Catheter Infection focused on measuring Catheter, Algorithms, Sepsis
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.
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
NCT ID
NCT04920877
First Posted
June 4, 2021
Last Updated
June 4, 2021
Sponsor
Abant Izzet Baysal University
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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