Viewing Study NCT06470100



Ignite Creation Date: 2024-07-17 @ 11:43 AM
Last Modification Date: 2024-10-26 @ 3:32 PM
Study NCT ID: NCT06470100
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-06-24
First Post: 2024-06-17

Brief Title: Dexamethasone vs Dexmedetomidine for ESPB in Pain Management After Knee Arthroplasty
Sponsor: Poznan University of Medical Sciences
Organization: Poznan University of Medical Sciences

Study Overview

Official Title: Dexamethasone vs Dexmedetomidine for ESPB in Pain Management After Total Knee Arthroplasty
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-06
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: Effect of perineurial dexamethasone and dexmedetomidine on erector spinal plane block duration for knee arthroplasty
Detailed Description: This study is proposed to explore the effect of perineurial Dexamethasone and Dexmedetomidine on erector spinal plane block duration for spine surgery

After spine surgery patients need good analgesia Peripheral nerve blocks have provided a safe effective method to control early postoperative pain when symptoms are most severe

Local anaesthesias much lower toxicity threshold makes it essential for its safety An effective adjuvant such as Dexamethasone or Dexmedetomidine could allow for a higher dilution of local anaesthetics while maintaining and enhancing their analgesic effect

There is considerable research comparing intravenous and perineural dexamethasone and Dexmedetomidine use in orthopaedic surgeries However there is a massive lack of research regarding knee surgery and the Erector Spine Plane Block

In this study investigators compare perineural Dexamethasone and Dexmedetomidine

The investigator aims to find a dexamethasone or dexmedetomidine that covers the need for good pain relief and fast recovery postoperatively

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