Decreasing leakage of continuous femoral nerve catheter fixation with 2-octyl cyanoacrylate glue (Dermabond®): A randomized controlled study

Phase 3

Completed

• Conditions: Total knee arthroplasty patients; Total knee arthroplasty; Catheter fixation; 2- octyl cyanoacryolate glue

• Registration Number: TCTR20200228002
• Lead Sponsor: /A

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2019-02-23
• Study Start: 2020-02-28
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Total knee arthroplasty patients
Age 40-80 years
ASA physical status 1-4

Exclusion Criteria

Localized infection at inguinal area
Allergy to LA drug/glue/adhesive glue
Refused to participate in the study

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Catheter leakage 24 and 48 hr after the operation Percentage

Secondary Outcome Measures

Name	Time	Method
Catheter migration 24 and 48 hr after the operation Percentage