Viewing Study NCT04544423



Ignite Creation Date: 2024-05-06 @ 3:11 PM
Last Modification Date: 2024-10-26 @ 1:44 PM
Study NCT ID: NCT04544423
Status: UNKNOWN
Last Update Posted: 2020-09-10
First Post: 2020-09-03

Brief Title: Lumbar Erector Spinae Plane Block in Knee Prosthesis
Sponsor: Tokat Gaziosmanpasa University
Organization: Tokat Gaziosmanpasa University

Study Overview

Official Title: Ultrasound-guided Lumbar Erector Spinae Plane Block For Postoperative Analgesia in Knee Prosthesis
Status: UNKNOWN
Status Verified Date: 2020-09
Last Known Status: NOT_YET_RECRUITING
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: To determine the postoperative analgesic efficiency of ultrasound-guided lumbar erector spinae plane block patients are divided into two groups Study group received ultrasound-guided lumbar erector spinae plane block where control had none Visual analog scale and opioid consumption are recorded
Detailed Description: Erector spinae plane block has successfully been demonstrated to provide an efficient analgesia in patients with rib fracture open thoracotomy breast surgery The present study is aimed to investigate the intraoperative hemodynamic responses anesthetic and analgesic consumption and postoperative recovery quality of erector spinae plane block in patients with knee prosthesis After approval patients enrolled in the study are divided into two groups by computer-based randomization technique as control and study group After standard monitorization anesthesia induction and tracheal intubation erector spinae plane block is performed to study group and no intervention to control group

In the intraoperative period 10 mg kg paracetamol and 005 mg kg morphine will be used for postoperative analgesia After surgery all patients will be given 10 mgkg paracetamol every 8 hours and will be fitted with a patient-controlled analgesia PCA device Tramadol HCL PCA device bolus dose will be set to 20 mg lock time will be set to 10 minutes and the number of buttons per hour will be set as 3for postoperative analgesiaAfter surgery VAS scores of the patients will be evaluated in the recovery room 13612 and 24 hours Patients with VAS4 will be given 003mg kg morphine as salvage analgesiaAfter 30 minutes the patients VAS will be re-evaluatedIf VAS4 the same dose will be repeated

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