Ignite Creation Date:
2024-05-06 @ 9:00 AM
Last Modification Date:
2024-10-26 @ 12:08 PM
Study NCT ID:
NCT02871713
Status:
COMPLETED
Last Update Posted:
2021-01-05
First Post:
2016-08-15
Brief Title:
A Randomized Controlled Trial Comparing Intrathecal Morphine with Quadratus Lumborum Block for Post-cesarean Delivery Analgesia
Sponsor:
Vishal Uppal
Organization:
Nova Scotia Health Authority
Study Overview
Official Title:
A Randomized Controlled Trial Comparing Intrathecal Morphine with Quadratus Lumborum Block As Part of a Multimodal Analgesia Strategy for Post-cesarean Delivery Analgesia
Status:
COMPLETED
Status Verified Date:
2024-09
Last Known Status:
RECRUITING
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:
Pain after caesarean delivery CD can interfere with the moms ability to look after her baby and may contribute to developing long term pain and disability Women having a CD receive pain medication morphine as part of their spinal anesthetic to help with pain relief after surgery Morphine works well however has several side effects such as nausea vomiting and itching which may be severe enough to make it difficult to care for herself and her new baby In some cases morphine causes difficulty in passing urine within first 24-hours of the CD requiring catheterization and thus restricting mobilization The quadratus lumborum block QLB is a newer nerve block that uses local anaesthetic solution to numb the nerves carrying pain sensation from surgical incision site QLB may be able to provide effective pain control without the side-effects associated with the spinal morphine This study is to determine if women receiving QLB have as good pain control with fewer side effects than those who do receive the spinal morphine Adequate pain control will be assessed by their pain scores and recovery in the 24 to 48 hours after CD The side effect profile of the two techniques quality of recovery and long term impact will also be compared during this study
In addition we would like to compare the patients who received both analgesic regimens ITM and QLB with patients who received only one analgesic intervention ie either ITM or QLB Further the study will help us answer if combining the two analgesic interventions if beneficial or not
In addition we would like to compare the patients who received both analgesic regimens ITM and QLB with patients who received only one analgesic intervention ie either ITM or QLB Further the study will help us answer if combining the two analgesic interventions if beneficial or not
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