Ignite Creation Date:
2024-07-17 @ 11:07 AM
Last Modification Date:
2024-10-26 @ 3:33 PM
Study NCT ID:
NCT06481462
Status:
RECRUITING
Last Update Posted:
2024-07-05
First Post:
2024-06-25
Brief Title:
Intrathecal Morphine vs US-Guided Bilateral Posterior Quadratus Lumborum Block in Cesarean Section
Sponsor:
Ondokuz Mayıs University
Organization:
Ondokuz Mayıs University
Study Overview
Official Title:
Comparison of the Effects of Intrathecal Morphine and Ultrasound-Guided Bilateral Posterior Quadratus Lumborum Block on Postoperative Acute Pain in Cesarean Section A Prospective Observational Study
Status:
RECRUITING
Status Verified Date:
2024-07
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:
In this study it was aimed to evaluate the effects of intrathecal morphine and posterior quadratus lumborum block QLB2 on postoperative acute pain scores and opioid consumption in the first 24 hours after cesarean section
Detailed Description:
Postoperative acute pain following a cesarean section is sharp well-localized and highly intense An ideal pain management approach after a cesarean section should provide high-quality analgesia with minimal side effects and facilitate the mothers rapid return to daily activities Different options for pain control include central blocks peripheral blocks and systemic medications
Intrathecal morphine ITM administration is a widely used approach for post-cesarean pain management both globally and in our clinic However it can reduce patient satisfaction due to side effects such as nausea vomiting and itching On the other hand the Quadratus Lumborum Block QLB a type of peripheral block has proven analgesic efficacy in controlling acute postoperative pain following a cesarean section The aim of this study is to examine and compare the analgesic efficacy of intrathecal morphine ITM and Posterior Quadratus Lumborum in the management of acute postoperative pain after a cesarean section
This study is a single-center double-blind prospective observational study
Patients will be divided into 2 groups
Group 1 The group receiving intrathecal morphine ITM
Group 2 The group receiving Posterior Quadratus Lumborum Block
In elective cesarean section cases under spinal anesthesia the patient group receiving ITM and posterior QLB will be evaluated for obstetric general well-being during the first 24 hours and at discharge Total morphine consumption in the first 24 hours Pain scores NRS at rest and during movement presence of nausea-vomiting and itching patient satisfaction and any potential side effects will be recorded through follow-up
Intrathecal morphine ITM administration is a widely used approach for post-cesarean pain management both globally and in our clinic However it can reduce patient satisfaction due to side effects such as nausea vomiting and itching On the other hand the Quadratus Lumborum Block QLB a type of peripheral block has proven analgesic efficacy in controlling acute postoperative pain following a cesarean section The aim of this study is to examine and compare the analgesic efficacy of intrathecal morphine ITM and Posterior Quadratus Lumborum in the management of acute postoperative pain after a cesarean section
This study is a single-center double-blind prospective observational study
Patients will be divided into 2 groups
Group 1 The group receiving intrathecal morphine ITM
Group 2 The group receiving Posterior Quadratus Lumborum Block
In elective cesarean section cases under spinal anesthesia the patient group receiving ITM and posterior QLB will be evaluated for obstetric general well-being during the first 24 hours and at discharge Total morphine consumption in the first 24 hours Pain scores NRS at rest and during movement presence of nausea-vomiting and itching patient satisfaction and any potential side effects will be recorded through follow-up
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