Status:
COMPLETED
Comparative Analysis of Incidence of Newly Developed Postoperative Low Back Pain with Field Block Versus Without Field-block Before Spinal Anaesthesia for Patients Undergoing Caesarean Sections
Lead Sponsor:
Tata Main Hospital
Conditions:
Caesarean Section
Eligibility:
FEMALE
18-45 years
Phase:
NA
Brief Summary
The study aimed to evaluate the effectiveness of field block in preventing postoperative low back pain (PDPB) in patients undergoing Cesarean Sections.
Detailed Description
The purpose of this study was to evaluate the effectiveness of field block with lidocaine 2% (5 ml) administered with a 24G hypodermic needle before spinal anesthesia for patients undergoing LSCS, in ...
Eligibility Criteria
Inclusion
- All patients undergoing LSCS under spinal anesthesia, ASA Grade 2 and Grade 2E and willing to participate in the trial
Exclusion
- Spine pathology/instability and coagulopathy, ASA Grade 3 and above, Pre-exiting low back pain, Morbid Obesity (BMI \> 35), Patients needing more than 1 attempt for administration of spinal anaesthesia, Patients utilizing labour analgesia, Local infection or inflammation at the site of spinal anesthesia/field block, Unwilling to participate
- \-
Key Trial Info
Start Date :
April 1 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 31 2024
Estimated Enrollment :
220 Patients enrolled
Trial Details
Trial ID
NCT06602505
Start Date
April 1 2023
End Date
March 31 2024
Last Update
September 19 2024
Active Locations (1)
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1
Tata Main Hospital
Jamshedpur, Jharkhand, India, 831011