Viewing Study NCT06125067



Ignite Creation Date: 2024-05-06 @ 7:46 PM
Last Modification Date: 2024-10-26 @ 3:13 PM
Study NCT ID: NCT06125067
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: 2024-03-15
First Post: 2023-11-04

Brief Title: Fascia Iliaca Compartment Block and iPACK Block in Total Knee Arthroplasty
Sponsor: Ankara Ataturk Sanatorium Training and Research Hospital
Organization: Ankara Ataturk Sanatorium Training and Research Hospital

Study Overview

Official Title: Comparison of the Efficacy of Fascia Iliaca Compartment Block and iPACK Block for Postoperative Analgesia in Total Knee Arthroplasty Operation
Status: ACTIVE_NOT_RECRUITING
Status Verified Date: 2024-07
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 investigators sought to compare the effectiveness of postoperative pain control between the standard intravenous multimodal analgesia procedure used in managing patients undergoing total knee surgery who experience severe postoperative analgesia needs and multimodal analgesia procedures that incorporate ultrasound-guided peripheral nerve blocks Fascia Iliaca Compartment Block or iPACK Block during postoperative follow-up The aim is to determine which procedure is more effective
Detailed Description: All patients who received a total knee replacement surgery conducted by orthopaedic surgeons at the operating theatre of Health Sciences University Ankara Atatürk Sanatorium Training and Research Hospital and underwent postoperative pain assessment by anaesthetists will be retrospectively reviewed as part of the study

Postoperative pain management follow-up for patients who have undergone surgical procedures at Anaesthesiology and Reanimation Clinic is standard practice during patients hospitalization Patients who have undergone painful and significant surgical procedures are typically given postoperative patient-controlled analgesia devices and are administered intravenous painkillers that are under the patients control As part of multimodal analgesia procedure the investigators apply peripheral nerve blocks routinely to eligible patients provided that the necessary criteria are met Once the postoperative Anesthesiology and Reanimation clinics follow-up form the regional anaesthesia follow-up form is completed patients receive coordinated follow-up care from anaesthesiologists and surgical physicians in postoperative ward to monitor analgesic requirements and increase patient satisfaction Hourly monitoring ensures that patients receive optimal care

The aims of study to examine the effectiveness of these procedures The investigators will include all patients who received elective total knee arthroplasty surgery in the operating room of Ankara Atatürk Sanatorium Training and Research Hospital within the past year between 01 March 2022 and 31 March 2023 in retrospective file review and postoperative pain follow-up study

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