Viewing Study NCT06519708



Ignite Creation Date: 2024-10-26 @ 3:35 PM
Last Modification Date: 2024-10-26 @ 3:35 PM
Study NCT ID: NCT06519708
Status: RECRUITING
Last Update Posted: None
First Post: 2024-07-21

Brief Title: Analgesic Efficacy of Erector Spinae Plane Block vs External Oblique Intercostal Plane Block in Subcostal Cancer Surgeries
Sponsor: None
Organization: None

Study Overview

Official Title: Analgesic Efficacy of Erector Spinae Plane Block vs External Oblique Intercostal Plane Block in Subcostal Cancer Surgeries A Randomized Controlled Study
Status: RECRUITING
Status Verified Date: 2024-07
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 evaluate the impact of ultrasound-guided erector spinae plane block compared to ultrasound-guided external oblique intercostal plane block regarding management of postoperative acute pain in patients undergoing above Umbilical surgical procedure
Detailed Description: Subcostal incisions in cancer surgeries as in hepatectomy and nephrectomy are a cause of severe pain and can lead to significant respiratory impairment Regional anesthesia of the trunk and abdominal wall is usually centered on epidural analgesia

Erector spinae plane block ESPB is the deposition of local anesthetic LA in the interfascial plane at the paraspinal region It provides effective visceral and somatic analgesia

The recently described external oblique intercostal plane block EOIPB is a simple effective and convenient block particularly in the context of morbid obesity at which local anesthetic LA is deposited in the interfacial plane deep to external oblique muscle at the sixth intercostal space It provides a blockade of the thoracoabdominal nerves at the level of T6 to T10

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