NCT03692559

Brief Summary

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

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
331

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Aug 2015

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 20, 2015

Completed
1.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 3, 2017

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 3, 2017

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

October 18, 2017

Completed
12 months until next milestone

First Posted

Study publicly available on registry

October 2, 2018

Completed
Last Updated

October 2, 2018

Status Verified

September 1, 2018

Enrollment Period

1.5 years

First QC Date

October 18, 2017

Last Update Submit

September 30, 2018

Conditions

Central Line-associated Bloodstream Infection (CLABSI)

Keywords

CRBSICLABSI

Outcome Measures

Primary Outcomes (1)

  • Catheter-related blood stream infections density after dressing change

    Confirm blood culture results and judge whether it is catheter related Bloodstream infection(CRBSI)

    up to 18 months

Secondary Outcomes (1)

  • Central Line-Associated Bloodstream Infection density after dressing change

    up to 18 months

Study Arms (2)

full sterile dressing

EXPERIMENTAL

Patients receive full sterile dressing

Other: full aseptic dressing

usual standard care

NO INTERVENTION

Patients receive usual standard care

Interventions

full aseptic dressingOTHER

Replacement of the central venous catheters in the dressing process

full sterile dressing

Eligibility Criteria

Age20 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

  • 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)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Officials

  • Meng-lan Teng

    National Taiwan University Hospital Hsin-Chu Branch

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Head Nurse

Study Record Dates

First Submitted

October 18, 2017

First Posted

October 2, 2018

Study Start

August 20, 2015

Primary Completion

February 3, 2017

Study Completion

February 3, 2017

Last Updated

October 2, 2018

Record last verified: 2018-09

Data Sharing

IPD Sharing
Will not share