Viewing Study NCT06088836



Ignite Creation Date: 2024-05-06 @ 7:38 PM
Last Modification Date: 2024-10-26 @ 3:11 PM
Study NCT ID: NCT06088836
Status: RECRUITING
Last Update Posted: 2023-10-19
First Post: 2023-10-03

Brief Title: Ultrasound- Guided Continuous Retro Laminar Block Versus Continuous Erector Spinae Plane Block in Multiple Rib Fractures
Sponsor: Tanta University
Organization: Tanta University

Study Overview

Official Title: Impact of Ultrasound- Guided Continuous Retro Laminar Block Versus Continuous Erector Spinae Plane Block on Incentive Spirometry Volumes and Pain Scores in Multiple Rib Fractures
Status: RECRUITING
Status Verified Date: 2023-10
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 the incentive spirometry volume and analgesic efficacy of ultrasound guided continuous Retrolaminar block and continuous Erector spinae plain block in patients with multiple rib fractures
Detailed Description: Thoracic epidural analgesia TEA and thoracic paravertebral block TPVB are strongly recommended techniques for managing thoracic neuropathic pain However they can be technically challenging to perform and are associated with up to 15 failure rate in Thoracic epidural analgesia TEAand potential risk of pneumothorax in thoracic paravertebral block TPVBNewer approaches have been the focus of many studies in recent years these approaches include retrolaminar block and erector spinae plane block

Retrolaminar block RLB is a new thoracic truncal block for controlling somatic pain in both the thoracic and abdominal walls

The Erector Spinae plane block ESPB has been used successfully to manage severe neuropathic pain arising from ribs The basis to use ESPB is its likely site of action which is the dorsal and ventral rami of the thoracic spinal nerves

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