Viewing Study NCT06599723



Ignite Creation Date: 2024-10-26 @ 3:40 PM
Last Modification Date: 2024-10-26 @ 3:40 PM
Study NCT ID: NCT06599723
Status: RECRUITING
Last Update Posted: None
First Post: 2024-09-12

Brief Title: Racz Catheter Technique Versus Conventional Technique in Lumbar Epidural Steroid Injection for Management of Low Back Pain
Sponsor: None
Organization: None

Study Overview

Official Title: Racz Catheter Technique Versus Conventional Technique in Lumbar Epidural Steroid Injection for Management of Low Back Pain A Randomized Controlled Trial
Status: RECRUITING
Status Verified Date: 2024-09
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: The aim of this study is to compare Racz catheter technique and conventional technique in lumbar epidural steroid injection for the management of low back pain
Detailed Description: Low back pain LBP is defined as a localized discomfort sensation below the costal margin and above the inferior gluteal folds with or without leg pain Conservative treatment for LBP is focused on delaying or preventing the need for surgery Indeed LBP can improve spontaneously or with non-surgical treatment However cases that fail to improve with conservative management may need to be considered for a surgical approach

The epidural injection is a well-founded anesthetic and analgesic technique moreover nowadays new technological devices can help anesthesiologists to learn and to administer it One of these devices is Racz catheter epidural adhesiolysis Racz catheter epidural adhesiolysis treatment addresses two issues the injectate always reaches the area being targeted also the injections are likely to loosen fibrotic adhesions which may be the main cause of the pain in some cases

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