Ignite Creation Date:
2024-05-06 @ 8:28 PM
Last Modification Date:
2024-10-26 @ 3:28 PM
Study NCT ID:
NCT06393530
Status:
RECRUITING
Last Update Posted:
2024-05-01
First Post:
2024-04-26
Brief Title:
Erector Spinae Plane Block for Cervical Spine Surgery
Sponsor:
Poznan University of Medical Sciences
Organization:
Poznan University of Medical Sciences
Study Overview
Official Title:
Erector Spinae Plane Block for Cervical Spine Surgery A Prospective Randomized Double-blinded Clinical Trial
Status:
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 study aims to assess the interfacial plane blocks effect on pain level course of postoperative rehabilitation and anti-inflammatory analgesic effect
Detailed Description:
This study evaluates the analgesic efficacy in adults of bilevel bilateral erector spinae plane ESP blocks after posterior cervical spinal fusion surgery by assessing postoperative pain scores and opiate requirements as the primary outcome measures We aim to investigate how ESP blocks performed under ultrasound guidance at the two vertebral levels contribute to postoperative pain control This will be determined by measuring numerical rating pain scores repeatedly following surgery and opiate consumption until the patient is discharged from the hospital These primary outcome measures will be compared between a treatment group of participants receiving ESP blocks and a control group receiving a sham block Our primary hypothesis is that ESP blocks significantly reduce postoperative pain and opiate requirements
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