Viewing Study NCT06436105



Ignite Creation Date: 2024-06-16 @ 11:49 AM
Last Modification Date: 2024-10-26 @ 3:30 PM
Study NCT ID: NCT06436105
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-05-30
First Post: 2024-05-24

Brief Title: COMPARISON OF PERIOPERATIVE ANALGESIC EFFECTIVENESS OF PATIENTS WHO HAD FASIA ILIAC COMPARTMENT BLOCK AND 4IN1 BLOCK APPLIED IN TOTAL KNEE PROSTHESIS SURGERY
Sponsor: Diskapi Yildirim Beyazit Education and Research Hospital
Organization: Diskapi Yildirim Beyazit Education and Research Hospital

Study Overview

Official Title: COMPARISON OF PERIOPERATIVE ANALGESIC EFFECTIVENESS OF PATIENTS WHO HAD FASIA ILIAC COMPARTMENT BLOCK AND 4IN1 BLOCK APPLIED IN TOTAL KNEE PROSTHESIS SURGERY
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-05
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: Patients who will undergo elective total knee arthroplasty surgery under spinal anesthesia will be included in the study according to the postoperative analgesia method applied Group Control Group FICB and Group 4in1 Peripheral nerve block will be performed with 30 ml 025 bupivacaine for Group FICB and Group 4 in 1 patients Peripheral nerve block will not be performed on Group Control patients Patient-controlled analgesia will be given to all three groups in the postoperative period PCA is a pain palliation method routinely used in all patients postoperatively NRS score PCA tramadol consumption PCA demand need for additional analgesia patient satisfaction nausea and vomiting will be monitored 24 hours postoperatively The aim of this study is to compare the perioperative analgesic effectiveness of patients who underwent fascia iliaca compartment block and 4 in 1 block in total knee arthroplasty surgery with each other and with the control group
Detailed Description: Total knee arthroplasty is a surgical procedure performed mostly on patients with osteoarthritis who have failed traditional conservative treatment Increasing knee osteoarthritis due to reasons such as life expectancy and body mass index causes this surgical procedure to be performed more frequently The knee joint which is innervated by the femoral obturator sciatic nerves and their branches has a complicated innervation and the pain following total knee arthrplasty is quite severe It is aimed to provide effective analgesia by blocking these nerves or terminal branches with various peripheral nerve blockade methods under USG guidance In recent years interest in studies aiming to block these nerves with a single injection has been increasing 4 in 1 block is a new technique applied from a single injection point to block the saphenous obturator sciatic and vastus medialis nerves that innervate the knee joint Fascia iliaca compartment block is a reliable technique applied from a single injection point to block the femoral lateral femoral cutaneous and obturator nerves behind the fascia iliaca

Patients who will undergo elective total knee arthroplasty surgery under spinal anesthesia will be included in the study according to the postoperative analgesia method applied Group Control Group FICB and Group 4in1 Peripheral nerve block will be performed with 30 ml 025 bupivacaine for Group FICB and Group 4 in 1 patients Peripheral nerve block will not be performed on Group Control patients Patient-controlled analgesia will be given to all three groups in the postoperative period PCA is a pain palliation method routinely used in all patients postoperatively NRS score PCA tramadol consumption PCA demand need for additional analgesia patient satisfaction nausea and vomiting will be monitored 24 hours postoperatively The aim of this study is to compare the perioperative analgesic effectiveness of patients who underwent fascia iliaca compartment block and 4 in 1 block in total knee arthroplasty surgery with each other and with the control group

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