Viewing Study NCT06382285



Ignite Creation Date: 2024-05-06 @ 8:27 PM
Last Modification Date: 2024-10-26 @ 3:27 PM
Study NCT ID: NCT06382285
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-04-24
First Post: 2023-09-07

Brief Title: The Effect of a Prolonged Peripheral Nerve Block on the Level of Pain After a Knee Replacement
Sponsor: Assaf-Harofeh Medical Center
Organization: Assaf-Harofeh Medical Center

Study Overview

Official Title: The Effect of a Prolonged Peripheral Nerve Block Utilazing Continuous Adductor Canal Block on the Level of Pain After a Knee Replacement Surgery
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-04
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 study is to examine the effect of a prolonged peripheral nerve block utilizing continuous adductor canal block on the level of pain after a knee replacement surgery
Detailed Description: Knee replacement surgery is one of the common orthopedic surgeries for the treatment of chronic knee pain The period after knee replacement surgery is accompanied by moderate to severe pain that affects the patients ability to quickly return to function Peripheral nerve blockers and analgesia of different types administered as part of the anesthesia process are optimal in controlling pain after surgery After the surgery the patients are admitted in the orthopedic inpatient department for 2-3 days on average after surgery for follow-up and early physical therapy necessary to achieve good results and return the patient to full function as soon as possible The level of pain greatly affects the success rate of the patients rehabilitation Thus since the duration of peripheral nerve block activity does not exceed 8-16 hours on average it is suggested to treat the patients with a prolonged peripheral nerve block utilizing continuous adductor canal block for 24 hours after surgery

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?: False
Is an FDA AA801 Violation?: None