Ignite Creation Date:
2024-05-06 @ 6:33 PM
Last Modification Date:
2024-10-26 @ 2:50 PM
Study NCT ID:
NCT05706285
Status:
COMPLETED
Last Update Posted:
2024-03-28
First Post:
2023-01-04
Brief Title:
Comparing Intrathecal Morphine With Erector Spina Plane Block in Open Gastrectomy Surgery
Sponsor:
Marmara University
Organization:
Marmara University
Study Overview
Official Title:
Comparing Postoperative Analgesic Effects of Intrathecal Morphine With Erector Spina Plane Block in Open Gastrectomy Surgery
Status:
COMPLETED
Status Verified Date:
2024-03
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:
Open gastrectomy causes severe postoperative pain due to wide surgical incisions retraction of the abdominal wall and direct manipulation of the visceral organs It leads to delayed postoperative recovery increased medical expenses and poor surgical outcomes Epidural analgesia intrathecal morphine and patient-controlled analgesia are frequently used in the postoperative pain management of abdominal surgeries Intrathecal morphine is applied as a standard protocol in many centers due to its ease of application and effective pain control However it has undesirable effects such as postoperative nausea-vomiting itching and most importantly respiratory depression Regional interfascial plane blocks such as erector spina plane block have recently been popular in clinical practice to provide postoperative pain control Erector spina plane block when placed preoperatively is expected to reduce opioid consumption and improve outcomes The primary implication of this study is to compare postoperative pain scores and opioid consumption It is also aimed to compare the effectiveness of Numeric Rating Scale and Clinically Aligned Pain Assessment Tool used in postoperative pain assesment
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?:
None