Comparison of securing the umbilical catheter using bridging method versus using transparent film dressing without bridging method : A Pilot Study

Phase 2

• Conditions: eonates who require the umbilical catheter insertion; umbilical catheter; skin injury; securement

• Registration Number: TCTR20240522005
• Lead Sponsor: Walaiporn Bowornkitiwong

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-05-22
• Last Update Posted: 19 August 2024
• Study Completion: 2025-04-30

Recruitment & Eligibility

• Status: Pending (Not yet recruiting)
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

1. Neonates who will receive the insertion of umbilical catheters, either umbilical artery catheters or umbilical venous catheters, 2. Admitted to neonatal intensive care unit, 3. Age 0-14 days

Exclusion Criteria

1. Neonates who failed umbilical catheter insertion, 2. Unstable vital signs or oxygen saturation

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Displacement of umbilical catheter during the umbilical catheter in situ centimeter

Secondary Outcome Measures

Name	Time	Method
Skin injury from umbilical catheter insertion until the removal of the umbilical catheter Adhesive-related skin injuries grading scale,Catheter related blood stream infection 48 hours after insertion until removal of the catheter positive hemoculture,Duration of securement A duration from the start of suture until the completion of the tape attachment minutes