Viewing Study NCT06573931



Ignite Creation Date: 2024-10-26 @ 3:38 PM
Last Modification Date: 2024-10-26 @ 3:38 PM
Study NCT ID: NCT06573931
Status: RECRUITING
Last Update Posted: None
First Post: 2024-08-24

Brief Title: Lumbar Erector Spinae Plane Block vs Fascia Iliaca Block vs Lumbar Plexus Block for Postoperative Analgesia for Total Hip Arthroplasty
Sponsor: None
Organization: None

Study Overview

Official Title: Lumbar Erector Spinae Plane Block vs Fascia Iliaca Block vs Lumbar Plexus Block for Postoperative Analgesia for Total Hip Arthroplasty A Randomized Clinical Trial
Status: RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study aims to compare lumbar erector spinae plane block fascia iliaca block and lumbar plexus block for postoperative analgesia for hip surgery
Detailed Description: Approximately 500000 hip arthroplasties are performed each year in the United States Traditionally this procedure has been performed under general anesthesia However neuraxial and regional anesthesia have become more commonly utilized to aid in postoperative analgesia and reduce the side effects of opioids namely sedation nausea and vomiting Postoperative pain control has a significant impact on earlier ambulation initiation of physical therapy better functional recovery and overall patient satisfaction

Lumbar erector spinae plane block LESPB was reported to lead to effective postoperative analgesia in hip and proximal femoral surgery

The fascia iliaca block FIB is an established and effective technique especially when US guidance and proximal approaches are used

lumbar plexus block LPB could be safe because of the targeted somatic nerve block in the psoas region which prevents dispensable sympathetic block even in cardiovascular-compromised patients

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None