Viewing Study NCT05910281



Ignite Creation Date: 2024-05-06 @ 7:09 PM
Last Modification Date: 2024-10-26 @ 3:01 PM
Study NCT ID: NCT05910281
Status: RECRUITING
Last Update Posted: 2023-07-24
First Post: 2023-06-09

Brief Title: Rebound Pain and Related Factors in Postoperative Patients With Total Knee Arthroplasty
Sponsor: Gulhane Training and Research Hospital
Organization: Gulhane Training and Research Hospital

Study Overview

Official Title: Rebound Pain and Related Factors in Patients Who Underwent Femoral Nerve Block for Postoperative Pain Control in Total Knee Arthroplasty
Status: 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 aim of this prospective observational study is to detect rebound pain and related factors in postoperative patients with total knee arthroplasty
Detailed Description: Total knee arthroplasty is an effective treatment method for knee osteoarthritis and because it is an invasive method more than 50 of patients experience postoperative pain Peripheral nerve blocks are widely used for optimal pain control The femoral block is a frequently preferred peripheral nerve block method for postoperative analgesia in total knee arthroplasty surgery However after peripheral nerve block a condition called rebound pain rebound pain which is described as very severe pain lasting about 2 hours usually of the burning type occurs The aim of this prospective observational study is to detect rebound pain and related factors in postoperative patients with total knee arthroplasty

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