Ultrasound-Guided QL Block Versus TAP Block For Post-Operative Pain In Lower Abdominal Surgeries
Ultrasound-Guided Quadratus Lumborum Block Versus Transversus Abdominis Plane Block For Post-Operative Pain In Lower Abdominal Surgeries In Adult Patients, Prospective, Comparative Randomized Study
1 other identifier
interventional
50
1 country
1
Brief Summary
This study aims to compare the efficacy of ultrasound-guided QL block and TAP block for postoperative pain management following lower abdominal surgeries.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable postoperative-pain
Started Apr 2025
Shorter than P25 for not_applicable postoperative-pain
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 14, 2025
CompletedFirst Submitted
Initial submission to the registry
May 10, 2025
CompletedFirst Posted
Study publicly available on registry
May 18, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 15, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
October 15, 2025
CompletedMay 18, 2025
April 1, 2025
6 months
May 10, 2025
May 10, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
efficacy of ultrasound-guided QL block and TAP block for postoperative pain management following lower abdominal surgeries.
Visual Analog Scale (VAS) at rest and at movement
48 hours after operation
Study Arms (2)
US Guided QL Block For Post-Operative Pain In Lower Abdominal Surgeries In Adult Patients
ACTIVE COMPARATORGroup ( 1 ) QLB "Type III": Patients will receive QLB performedwith20ml of diluted bupivacaine 0.25% on each side.
US Guided TAP Block For Post-Operative Pain In Lower Abdominal Surgeries In Adult Patients
ACTIVE COMPARATORGroup ( 2 ) TAP: Patients will receive TAP block performed with 20ml of diluted bupivacaine 0.25% on each side.
Interventions
Group ( 1 ) QLB "Type III": Patients will receive QLB performedwith20ml of diluted bupivacaine 0.25% on each side.
Group ( 2 ) TAP: Patients will receive TAP block performed with 20ml of diluted bupivacaine 0.25% on each side.
Eligibility Criteria
You may qualify if:
- patients aged from 18 to 65 years old.
- American Society of Anesthesiologists (ASA) physical status I - II.
- Patients scheduled for elective lower abdominal surgery.
You may not qualify if:
- Patient refusal.
- Patients with BMI (body mass index) \> 35 kg.m-2 , \[morbid obesity\].
- Patients with significant neurological, psychatric or neuromascular disease.
- Patients had local skin infection at the block injection site.
- Patients who operated under epidural and patient-controlled analgesia \[PCA\].
- Sensitivity to prescribed analgesia.
- Coagulopathies or those who had uncontrolled chronic medical disease \[e.g. diabetes mellitus, hypertension, or cardiac diseases\].
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Sohag Universitylead
Study Sites (1)
Sohag University Hospital
Sohag, Egypt
Related Publications (3)
Borglum J, Gogenur I, Bendtsen TF. Abdominal wall blocks in adults. Curr Opin Anaesthesiol. 2016 Oct;29(5):638-43. doi: 10.1097/ACO.0000000000000378.
PMID: 27429253BACKGROUNDWick EC, Grant MC, Wu CL. Postoperative Multimodal Analgesia Pain Management With Nonopioid Analgesics and Techniques: A Review. JAMA Surg. 2017 Jul 1;152(7):691-697. doi: 10.1001/jamasurg.2017.0898.
PMID: 28564673BACKGROUNDChen Q, Beal EW, Okunrintemi V, Cerier E, Paredes A, Sun S, Olsen G, Pawlik TM. The Association Between Patient Satisfaction and Patient-Reported Health Outcomes. J Patient Exp. 2019 Sep;6(3):201-209. doi: 10.1177/2374373518795414. Epub 2018 Aug 27.
PMID: 31535008BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Resident, Anesthesiology, Surgical ICU and Pain Medicine, Faculty of Medicine, Sohag University
Study Record Dates
First Submitted
May 10, 2025
First Posted
May 18, 2025
Study Start
April 14, 2025
Primary Completion
October 15, 2025
Study Completion
October 15, 2025
Last Updated
May 18, 2025
Record last verified: 2025-04