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The Effects of Different Ways of Dressing Central Line Associated Bloodstream Infections

N

National Taiwan University Hospital Hsin-Chu Branch

Status

Completed

Conditions

Central Line-associated Bloodstream Infection (CLABSI)

Treatments

Other: full aseptic dressing

Study type

Interventional

Funder types

Other

Identifiers

NCT03692559
104-032-E

Details and patient eligibility

About

The goal of our study was to investigate whether different methods of dressing could lower catheter-associated bloodstream infections.

Full description

The study method was experimental in design and recruited 331 medical intensive care unit patients with placement of central catheters in one regional hospital in northern Taiwan. The investigators used block randomization to assign patients to the study group or control group. In study group which included 163 participants, the investigators used aseptic coverings during dressing and in the control group which included 168 participants the process of dressing was as routine. Study period started from the first day of catheter insertion and ends with either the removal of catheter or discharge from intensive care unit. The investigators defined the infection outcome according to culture results, and the guidelines by Infectious Diseases Society of America and Centers for Disease Control and Prevention, USA. Analysis was done by SPSS version 23. The investigators used percentage and average to study characteristics of participants. The investigators used Chi-Square or Fisher's exact test and Poisson distribution to analyze the incidence rate of bloodstream infections and the infection density. The investigators used Kaplan-Meier curve to demonstrate the catheter infection-free days and the catheter redness symptoms days of the two groups. The investigators used logistic regression model to analyze factors associated with development of bloodstream infections.

Enrollment

331 patients

Sex

All

Ages

20+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adults older than 20 years old
  • Patients with central venous catheters
  • Agree to participate in this study, and fill out the study consent

Exclusion criteria

  • PICC patients placed
  • Patients with bloodstream infection
  • Patients with immunocompromised patients (such as HIV, AIDS, pregnant, or cancer patients who are receiving chemotherapy or radiotherapy)

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

331 participants in 2 patient groups

full sterile dressing
Experimental group
Description:
Patients receive full sterile dressing
Treatment:
Other: full aseptic dressing
usual standard care
No Intervention group
Description:
Patients receive usual standard care

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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