Viewing Study NCT06935006


Ignite Creation Date: 2025-12-26 @ 3:59 PM
Ignite Modification Date: 2025-12-31 @ 6:39 PM
Study NCT ID: NCT06935006
Status: NOT_YET_RECRUITING
Last Update Posted: 2025-04-18
First Post: 2025-03-09
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Erector Spinae Block vs Conventional Analgesia for Postoperative Analgesia in PCNL
Sponsor: Sohag University
Organization:

Study Overview

Official Title: Sonographic Guided Erector Spinae Plane Block Versus Conventional Analgesia After Percutaneous Nephrolithotomy a Comparative Randomized Study
Status: NOT_YET_RECRUITING
Status Verified Date: 2025-04
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: 50 adult patients scheduled for percutaneous nephrolithotomy in Sohag university hospitals will be devided in two groups one of them will receive Sonographic guided erector spinae plane block using 20 ml volume of bupivacaine 0.25 percent and the other will receive conventional analgesia of 0.1 mg/kg IV morphine
Detailed Description: None

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?: