Viewing Study NCT05961085



Ignite Creation Date: 2024-05-06 @ 7:18 PM
Last Modification Date: 2024-10-26 @ 3:04 PM
Study NCT ID: NCT05961085
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: 2024-01-12
First Post: 2023-07-11

Brief Title: Incidence of Adductor Canal Catheter Dislodgment
Sponsor: Sunnybrook Health Sciences Centre
Organization: Sunnybrook Health Sciences Centre

Study Overview

Official Title: Positioning of Continuous Adductor Canal Catheters After Total Knee Arthroplasty
Status: ACTIVE_NOT_RECRUITING
Status Verified Date: 2023-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this observational study is to determine the incidence of dislodgement for adductor canal catheters after total knee arthroplasty on post-operative day 1 We will also attempt to identify factors associated with secondary catheter failure
Detailed Description: Total knee arthroplasty TKA is a common procedure for indications including osteoarthritis and malignancy involving the knee with over 55285 knee replacements performed between 2020-2021 in Canada Ultrasound guided continuous adductor canal block cACB is the standard of care for postoperative analgesia for this procedure The catheter is not always as effective at providing analgesia as would be expected - which could be due to displacement of the catheter This displacement is most likely to occur peri-operatively or during physiotherapy post-operatively and as such post-operative assessments can provide useful insight into causes of secondary failure This prospective observational study aims to estimate the cACB dislodgment on POD 1 rate at a high volume tertiary care referral centre and identify factors associated with dislodgement and clinical sequelae As this is an observationalQI study of the current standard of care at Sunnybrook Health Sciences Centre anesthesiologists are free to use the cross sectional versus parallel insertion of the cACB per their discretion

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None