Viewing Study NCT06382376



Ignite Creation Date: 2024-05-06 @ 8:26 PM
Last Modification Date: 2024-10-26 @ 3:27 PM
Study NCT ID: NCT06382376
Status: COMPLETED
Last Update Posted: 2024-04-26
First Post: 2024-04-20

Brief Title: The Effect of Analgesia Methods Applied in Gynecological Cancer Surgeries on Postoperative Analgesia
Sponsor: Bakirkoy Dr Sadi Konuk Research and Training Hospital
Organization: Bakirkoy Dr Sadi Konuk Research and Training Hospital

Study Overview

Official Title: Four-quadrant Transversus Abdominis Plane Block Versus Intrathecal Morphine in Gynecological Cancer Surgeries a Single-center Retrospective Study
Status: COMPLETED
Status Verified Date: 2024-04
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: The aim of this study is to compare the effectiveness of intrathecal morphine and four-quadrant transversus abdominis plane block applied for postoperative analgesia in gynecological cancer surgeries

The key questions it aims to answer are

Is intrathecal morphine more effective in postoperative analgesia Patients who underwent gynecological cancer surgery were examined retrospectively The investigators evaluated the effect of intrathecal morphine and four-quadrant transversus abdominis plane block applied for postoperative analgesia on pain scores and postoperative opioid use
Detailed Description: Our study was designed retrospectively The investigators evaluated analgesia methods in patients who underwent laparoscopic or open surgery due to gynecological cancer between June 2023 and December 2023 The investigators evaluated the effect of intrathecal morphine and four-quadrant transversus abdominis plane block on postoperative analgesia and opioid use

Group 1 Intrathecal morphine administered group Group 2 Four quadrant transversus abdominis plane block applied group

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