Viewing Study NCT06239038



Ignite Creation Date: 2024-05-06 @ 8:02 PM
Last Modification Date: 2024-10-26 @ 3:19 PM
Study NCT ID: NCT06239038
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: 2024-02-06
First Post: 2024-01-25

Brief Title: Does Electrocautery Increase Postoperative Pain in Primary Total Knee Arthroplasty
Sponsor: Police General Hospital Thailand
Organization: Police General Hospital Thailand

Study Overview

Official Title: Does Electrocautery Increase Postoperative Pain in Primary Total Knee Arthroplasty A Randomized Controlled Trial
Status: ACTIVE_NOT_RECRUITING
Status Verified Date: 2024-02
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: Total knee arthroplasty TKA is a successful treatment for end-stage osteoarthritis of the knee The main advantages of TKA are to relieve the pain of the knee improve the knee function restore lower limb alignment and improve the quality of life for patients During TKA some surgeons prefer using a scalpel while others using electrocautery to expose the articular cavity Whether the use of scalpel can lead to better and faster recovery after the primary TKA is still controversial

The aim of this study was to compare the clinical outcomes of using the scalpel and the electrocautery in primary TKA
Detailed Description: A randomized controlled trial of patients underwent primary TKA between October 2021 and October 2023 The groups will be determined by using the computer to generate a randomization lists A total 132 patients were included with 66 patients in the scalpel group 66 patients in the electrocautery group All patients were evaluated using primary outcome Post-operative Visual Analog Scale VAS of pain secondary outcome estimated blood loss and Knee Injury and Osteoarthritis Outcome Score KOOS-JR

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