Viewing Study NCT06270654



Ignite Creation Date: 2024-05-06 @ 8:09 PM
Last Modification Date: 2024-10-26 @ 3:21 PM
Study NCT ID: NCT06270654
Status: RECRUITING
Last Update Posted: 2024-02-21
First Post: 2023-08-28

Brief Title: Management of Perioperative Pain Using Erector Spinae Plane Block in Open Microscopic Lumbar Surgery
Sponsor: University of Malaya
Organization: University of Malaya

Study Overview

Official Title: Management of Perioperative Pain Using Erector Spinae Plane Block in Open Microscopic Lumbar Surgery
Status: RECRUITING
Status Verified Date: 2024-02
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 compare patients receiving bilateral erector spinae block with ropivacaine vs control group in terms of pain score total opioid consumption hemodynamic changes intraoperatively length of hospitalisation time to ambulation post surgery and quality of recovery
Detailed Description: Most open spine surgery exacts a high degree of postsurgical pain due to the incision and muscle dissection of the vertebra The postoperative pain control and early mobilization improve the quality of the surgical care Inadequate pain relief might result in perioperative morbidity resulting in prolonged hospital stays

Erector spinae plane block ESPB is an interfascial plane block where local anaesthetic is injected in a plane preferably below the erector spinae muscle It can provide thoracic abdominal and even some lower extremity analgesia It was also theorised that erector spinae plane block can reduce opioid use and provide analgesia for lumbar surgery The financial cost that is saved by reducing the length of hospital stay perioperative morbidity will warrant the use of erector spinae plane block in patients undergoing lumbar spine 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