Viewing Study NCT06424938



Ignite Creation Date: 2024-06-16 @ 11:47 AM
Last Modification Date: 2024-10-26 @ 3:30 PM
Study NCT ID: NCT06424938
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-07-03
First Post: 2024-05-14

Brief Title: Postoperative Analgesia in Major Gynecological Cancer Surgeries
Sponsor: Duygu Akyol
Organization: Bakirkoy Dr Sadi Konuk Research and Training Hospital

Study Overview

Official Title: The Effect of Epidural Analgesia and Erector Spinae Plane Block on Intraoperative and Early Postoperative Outcomes in Open Gynecological Oncological Surgeries a Prospective Randomized Study
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: The aim of this study is to compare the effectiveness of epidural block or erector spinae plane block applied for postoperative analgesia in gynecological cancer surgeries

The main questions it aims to answer are

Is erector spinae plane block as effective as epidural block in postoperative analgesia The study was designed as a prospective randomized study Researchers evaluated the effects of epidural block or erector spinae plane block applied for postoperative analgesia on pain scores postoperative opioid use and mobilization in patients undergoing gynecological cancer surgery
Detailed Description: Our study was designed as a prospective randomized study The investigators evaluated the analgesia methods used in patients undergoing surgery for gynecologic cancer between May 2024 and December 2024 The investigators evaluated the effect of epidural block or erector spina plan block on postoperative analgesia opioid use and mobilization

Group 1 Epidural block group Group 2 Group with erector spina plan block

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