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Lateral Quadratus Lumborum Block Versus Transversus Abdominis Plane Block in Laparoscopic Surgery

Primary Purpose

Abdominal Pain

Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Ultrasound guided QL block
Ultrasound guided TAP block
Sponsored by
Fayoum University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Abdominal Pain focused on measuring laparoscopy, QL block, TAP block

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients scheduled for elective laparoscopic abdominal surgeries (inguinal hernia repair-missed IUCD extraction-appendectomy-ovarian vein ligation)
  • Patient aged 18-60 years
  • American Society of Anesthesiologists Physical Status I or II.

Exclusion Criteria:

  • Patient refusal
  • Body mass index (BMI) > 40 kilogram/square meter
  • Contraindication to regional anesthesia (coagulopathy, allergy to local anesthetic, sever thrombocytopenia or infection at puncture site)
  • Sepsis
  • Chronic pain condition requiring the intake of opioids at home
  • Any significant neurological, cardiovascular or respiratory disease.

Sites / Locations

  • Fayoum University hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

QL block group

TAP block group

Arm Description

For the ultrasound-guided quadratus lumborum block group, the patient was placed in lateral position . QL was identified medial to the aponeurosis of transversus abdominis muscle. Then the needle was inserted from supero-anterior to postero-inferior and advanced using in plane technique till the needle tip reached the anterolateral border of the QL at its junction with transversalis fascia.An injection of 20 mL of 0.25% bupivacaine was applied bilaterally

For the ultrasound-guided TAP block,The probe was placed in the mid-axillary line above the level of the anterior superior iliac spine, then slided cranially till the three abdominal wall muscles identified (External oblique muscle (EAO), internal oblique muscle (IOM) and transverse abdominis muscle (TAM)). The needle was advanced using in-plane technique till it reached the transvers abdominis plane. An injection of 20 mL of 0.25% bupivacaine was applied bilaterally

Outcomes

Primary Outcome Measures

The total morphine consumption at first 24 hours postoperatively
amount of morphine used in milligram after each block

Secondary Outcome Measures

Postoperative pain, assessed using visual analog scale (VAS) score at 30 min postoperatively.
from 0 to 10 degrees
Postoperative pain, assessed using visual analog scale (VAS) score at 2 h postoperatively.
from 0 to 10 degrees
Postoperative pain, assessed using visual analog scale (VAS) score at 4 h postoperatively.
from 0 to 10 degrees
Postoperative pain, assessed using visual analog scale (VAS) score at 6 h postoperatively.
from 0 to 10 degrees
Postoperative pain, assessed using visual analog scale (VAS) score at 12 h postoperatively.
from 0 to 10 degrees
Postoperative pain, assessed using visual analog scale (VAS) score at 24 h postoperatively.
from 0 to 10 degrees
Time to the first analgesic request
defined as the time interval elapsed between recovery and the first dose of morphine given.
frequency of patients required postoperative opioid.
in numbers
incidence of postoperative nausea and vomiting
Any postoperative nausea or vomiting related to morphine consumption
incidence of postoperative pruritus
Any postoperative pruritus related to morphine consumption
incidence of postoperative sedation at 30 min postoperatively
sedation was assessed with a five-point sedation scale
incidence of postoperative sedation at 2 h postoperatively
sedation was assessed with a five-point sedation scale
incidence of postoperative sedation at 6 h postoperatively
sedation was assessed with a five-point sedation scale
incidence of postoperative sedation at 12 h postoperatively
sedation was assessed with a five-point sedation scale
incidence of postoperative sedation at 24 h postoperatively
sedation was assessed with a five-point sedation scale
incidence of local anesthetic systemic toxicity
any observed local anesthetic systemic toxicity manifestations including CNS or CVS manifestations
incidence of vascular injury
incidence of vascular injury after each block
incidence of local hematoma
incidence of local hematoma at injection site after each block
incidence of visceral injury
incidence of visceral injury after each block

Full Information

First Posted
September 5, 2020
Last Updated
September 12, 2020
Sponsor
Fayoum University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04553991
Brief Title
Lateral Quadratus Lumborum Block Versus Transversus Abdominis Plane Block in Laparoscopic Surgery
Official Title
Analgesic Effect of Ultrasound-Guided Bilateral Quadratus Lumborum Block (Lateral Approach) Versus Bilateral Transversus Abdominis Plane Block With General Anesthesia in Laparoscopic Abdominal Surgery (Randomized Controlled Clinical Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
July 1, 2019 (Actual)
Primary Completion Date
February 1, 2020 (Actual)
Study Completion Date
May 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fayoum University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The transversus abdominis plane (TAP) block is an already established technique and is considered now as an efficient part of the multimodal pain management approach for abdominal surgical procedures. The quadratus lumborum block (QLB) is a recently described regional block that was first described by Blanco et al , which has been reported to provide an effective analgesia for upper and lower abdominal surgeries. The aim of this study is to compare the analgesic efficacy of TAP block and QLB 1 after laparoscopic abdominal surgery regarding opioid consumption, duration of analgesia and visual analog score. This prospective randomized controlled observer-blinded study compared between the analgesic efficacy between TAP block (n=25) versus QL block (n=25) in patients aged (18-60) years of American society of anesthesiologists physical status class I & II scheduled for elective laparoscopic abdominal surgical procedures. The primary outcome was the cumulative morphine consumption at first 24 hours postoperatively. Secondary outcomes included VAS scores, first analgesic requirements and any postoperative complications
Detailed Description
This prospective randomized, observer-blinded paralleled groups study was conducted following the tents of the Declaration of Helsinki. This study was approved by the local institutional ethics committee and local institutional review board of Fayoum university hospital and written informed consent was obtained from 50 adult patients scheduled for elective laparoscopic abdominal surgical procedures (inguinal hernia repair-missed IUCD extraction-appendectomy-ovarian vein ligation) between July 2019 and February 2020. Patients were randomly allocated into two groups (QLB group n=25 and TAPB group n=25) using computer generated random numbers kept in separate opaque envelopes that were opened by the study investigator just before the block. The patient and the data collector were unaware of the group allocation till the end of the study. Pre-operative assessment (History, examination and investigations) was done (according to the local protocol designed to evaluate the patients). Demographic characteristics: age, weight, height and BMI were recorded in preoperative assessment of patients. All patients received 150 mg Ranitidine oral tablet at night and on the morning just before the operation as a premedication. Before surgery, the participants received education about the VAS pain score (0-10) (where 0 = no pain and 10 = worst comprehensible pain) and the details of the nerve block procedures. After a 6 hrs fasting, the patients were taken to the operation theatre. Upon arrival to the operating room standard monitors (Pulse oximeter, noninvasive blood pressure monitoring, capnography and electrocardiogram) were applied and continued all over the operation, an 18 gauge peripheral intravenous (IV) cannula was inserted, IV midazolam 0.03 mgkg-1, metoclopramide 10 mg, and ceftriaxone 1 gm were administered to all patients as premedication then pre-oxygenation with O2 100% for at least 3 min then induction of anesthesia was done with fentanyl 1μgkg-1, propofol 1.5-2 mgkg-1 and atracurium 0.5 mgkg-1. Anesthesia was maintained by volume controlled ventilation (VCV) tidal volume 6-8 mlkg-1 with oxygen and air (50:50) with target of EtCO2≈ 35-40 mmHg, isoflurane 1:1.5 % volume concentration and atracurium 0.1 mgkg-1 every 20-30 minutes. The study solution was prepared in two syringes each contained 20 ml of bupivacaine 0.25%. By the end of surgery and before recovery from general anesthesia, either blocks were done using a high-frequency ultrasound probe Active Array L12-4 (8-13MHz) of an ultrasound machine (Philips clear vue350, Philips healthcare, Andover MA01810, USA) and a 22-gauge, 50 mm echogenic needle (Stimuplex D; B Braun, Germany). For the ultrasound-guided quadratus lumborum block group, the patient was placed in lateral position and skin sterilization was done with povidone iodine. Then a high frequency linear probe was placed above the iliac crest to recognize the three layers of the abdominal wall muscles. Transversus abdominis was traced posteriorly until the transversus aponeurosis appeared, then the probe tilted slightly caudal to enhance the appearance of transversus aponeurosis. QL was identified medial to the aponeurosis of transversus abdominis muscle. Then the needle was inserted from supero-anterior to postero-inferior and advanced using in plane technique till the needle tip reached the anterolateral border of the QL at its junction with transversalis fascia. After negative aspiration (to exclude intravascular injection), the correct needle position was confirmed by hydrodissection using 1mL of normal saline. Then 20 mL of 0.25% bupivacaine was applied. The same technique was performed on the other side. For the ultrasound-guided TAP block, skin sterilization was done with povidone iodine. The probe was placed in the mid-axillary line above the level of the anterior superior iliac spine, then slided cranially till the three abdominal wall muscles identified (External oblique muscle (EAO), internal oblique muscle (IOM) and transverse abdominis muscle (TAM)). The needle was advanced using in-plane technique till it reached the transvers abdominis plane between the IOM and TAM, the correct needle position was proved by hydrodissection using 1 mL of normal saline. An injection of 20 mL of 0.25% bupivacaine was applied. The same technique was performed on the other side. After performing the block anesthesia was discontinued and tracheal extubation was done once the patient fulfilled the extubation criteria. Patients were transferred to post-anesthetic care unit (PACU), where they were discharged from the PACU after a modified Aldrete score≥9. Visual analogue scale (VAS) was used to assess postoperative pain. All patients received analgesics according to the local institutional protocol as following (paracetamol 1gm IV infusion/8 hrs and ketorolac 30 mg IM/12 hrs.). A postoperative rescue analgesia with morphine sulfate IV was given to patients with VAS >4 at a bolus dose of 3 mg increments with a maximum dose of 15mg per 4 hours or 45mg per 24 hours. Sample size was estimated using G*Power© software version 3.1.9.2 (Institute of experimental psychology, Heinrich Heine University, Dusseldorf, Germany)149 with total opioid consumption among the two groups as the main primary outcome. Previous similar researches150 demonstrated that the effect size between the two groups was expected to be large of 1.12 and it calculated that 42 patients (21 patients per group) would provide to achieve a power of 95% with type I error rate of 0.05. However, we assigned 50 patients (25 patients per group) to compensate for data loss. The collected data were organized, tabulated and statistically analyzed using SPSS software statistical computer package version 22 (SPSS Inc, USA). Data were tested for normality using shapiro-wilks test. Numerical variables such as age, body weight, height and BMI were normally distributed and were described as mean ± standard deviation (SD). An independent t-test was used to compare the mean values of the two groups. Other variables were not normally distributed and were presented as median and interquartile range (IQR); Mann-Whitney U test was used as a test of significance. The time-to-event variable (time to analgesic request) was evaluated using the Kaplan-Meier method, and the logrank test was used to compare the groups. Qualitative data were presented as numbers and percentages, and the chi-squared test was used to determine significance. A two-sided P-value of <0.05 was considered statistically significant.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Abdominal Pain
Keywords
laparoscopy, QL block, TAP block

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
QL block group
Arm Type
Active Comparator
Arm Description
For the ultrasound-guided quadratus lumborum block group, the patient was placed in lateral position . QL was identified medial to the aponeurosis of transversus abdominis muscle. Then the needle was inserted from supero-anterior to postero-inferior and advanced using in plane technique till the needle tip reached the anterolateral border of the QL at its junction with transversalis fascia.An injection of 20 mL of 0.25% bupivacaine was applied bilaterally
Arm Title
TAP block group
Arm Type
Active Comparator
Arm Description
For the ultrasound-guided TAP block,The probe was placed in the mid-axillary line above the level of the anterior superior iliac spine, then slided cranially till the three abdominal wall muscles identified (External oblique muscle (EAO), internal oblique muscle (IOM) and transverse abdominis muscle (TAM)). The needle was advanced using in-plane technique till it reached the transvers abdominis plane. An injection of 20 mL of 0.25% bupivacaine was applied bilaterally
Intervention Type
Procedure
Intervention Name(s)
Ultrasound guided QL block
Intervention Description
20 mL of 0.25% bupivacaine was applied bilaterally at the anterolateral border of the QL at its junction with transversalis fascia
Intervention Type
Procedure
Intervention Name(s)
Ultrasound guided TAP block
Intervention Description
20 mL of 0.25% bupivacaine was applied bilaterally in the TAP
Primary Outcome Measure Information:
Title
The total morphine consumption at first 24 hours postoperatively
Description
amount of morphine used in milligram after each block
Time Frame
24 hours postoperatively
Secondary Outcome Measure Information:
Title
Postoperative pain, assessed using visual analog scale (VAS) score at 30 min postoperatively.
Description
from 0 to 10 degrees
Time Frame
30 minutes postoperatively
Title
Postoperative pain, assessed using visual analog scale (VAS) score at 2 h postoperatively.
Description
from 0 to 10 degrees
Time Frame
2 hours postoperatively
Title
Postoperative pain, assessed using visual analog scale (VAS) score at 4 h postoperatively.
Description
from 0 to 10 degrees
Time Frame
4 hours postoperatively
Title
Postoperative pain, assessed using visual analog scale (VAS) score at 6 h postoperatively.
Description
from 0 to 10 degrees
Time Frame
6 hours postoperatively
Title
Postoperative pain, assessed using visual analog scale (VAS) score at 12 h postoperatively.
Description
from 0 to 10 degrees
Time Frame
12 hours postoperatively
Title
Postoperative pain, assessed using visual analog scale (VAS) score at 24 h postoperatively.
Description
from 0 to 10 degrees
Time Frame
24 hours postoperatively
Title
Time to the first analgesic request
Description
defined as the time interval elapsed between recovery and the first dose of morphine given.
Time Frame
24 hours postoperatively
Title
frequency of patients required postoperative opioid.
Description
in numbers
Time Frame
First 24 hours postoperatively
Title
incidence of postoperative nausea and vomiting
Description
Any postoperative nausea or vomiting related to morphine consumption
Time Frame
First 24 hours postoperatively
Title
incidence of postoperative pruritus
Description
Any postoperative pruritus related to morphine consumption
Time Frame
First 24 hours postoperatively
Title
incidence of postoperative sedation at 30 min postoperatively
Description
sedation was assessed with a five-point sedation scale
Time Frame
at 30 minutes postoperatively
Title
incidence of postoperative sedation at 2 h postoperatively
Description
sedation was assessed with a five-point sedation scale
Time Frame
at 2 hours postoperatively
Title
incidence of postoperative sedation at 6 h postoperatively
Description
sedation was assessed with a five-point sedation scale
Time Frame
at 6 hours postoperatively
Title
incidence of postoperative sedation at 12 h postoperatively
Description
sedation was assessed with a five-point sedation scale
Time Frame
at 12 hours postoperatively
Title
incidence of postoperative sedation at 24 h postoperatively
Description
sedation was assessed with a five-point sedation scale
Time Frame
at 24 hours postoperatively
Title
incidence of local anesthetic systemic toxicity
Description
any observed local anesthetic systemic toxicity manifestations including CNS or CVS manifestations
Time Frame
in the first 24 hours postoperatively
Title
incidence of vascular injury
Description
incidence of vascular injury after each block
Time Frame
in the first 24 hours postoperatively
Title
incidence of local hematoma
Description
incidence of local hematoma at injection site after each block
Time Frame
in the first 24 hours postoperatively
Title
incidence of visceral injury
Description
incidence of visceral injury after each block
Time Frame
in the first 24 hours postoperatively
Other Pre-specified Outcome Measures:
Title
Patient's age
Description
In years
Time Frame
15 minutes before operation
Title
Patient's weight
Description
In kilograms
Time Frame
15 minutes before operation
Title
Patient's height
Description
In meters
Time Frame
15 minutes before operation
Title
Body mass index
Description
In kilogram/ square meter
Time Frame
15 minutes before operation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients scheduled for elective laparoscopic abdominal surgeries (inguinal hernia repair-missed IUCD extraction-appendectomy-ovarian vein ligation) Patient aged 18-60 years American Society of Anesthesiologists Physical Status I or II. Exclusion Criteria: Patient refusal Body mass index (BMI) > 40 kilogram/square meter Contraindication to regional anesthesia (coagulopathy, allergy to local anesthetic, sever thrombocytopenia or infection at puncture site) Sepsis Chronic pain condition requiring the intake of opioids at home Any significant neurological, cardiovascular or respiratory disease.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maged L boules, MD
Organizational Affiliation
Faculty of medicine, Fayoum university
Official's Role
Study Chair
Facility Information:
Facility Name
Fayoum University hospital
City
Madīnat Al Fayyūm
State/Province
Fayoum Governorate
ZIP/Postal Code
63514
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30662131
Citation
Kumar GD, Gnanasekar N, Kurhekar P, Prasad TK. A Comparative Study of Transversus Abdominis Plane Block versus Quadratus Lumborum Block for Postoperative Analgesia following Lower Abdominal Surgeries: A Prospective Double-blinded Study. Anesth Essays Res. 2018 Oct-Dec;12(4):919-923. doi: 10.4103/aer.AER_158_18.
Results Reference
background
PubMed Identifier
29929169
Citation
Okmen K, Metin Okmen B, Topal S. Ultrasound-guided posterior quadratus lumborum block for postoperative pain after laparoscopic cholecystectomy: A randomized controlled double blind study. J Clin Anesth. 2018 Sep;49:112-117. doi: 10.1016/j.jclinane.2018.06.027. Epub 2018 Jun 18.
Results Reference
background
PubMed Identifier
35386840
Citation
Fargaly OS, Boules ML, Hamed MA, Aleem Abbas MA, Shawky MA. Lateral Quadratus Lumborum Block versus Transversus Abdominis Plane Block in Laparoscopic Surgery: A Randomized Controlled Study. Anesthesiol Res Pract. 2022 Mar 28;2022:9201795. doi: 10.1155/2022/9201795. eCollection 2022.
Results Reference
derived

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Lateral Quadratus Lumborum Block Versus Transversus Abdominis Plane Block in Laparoscopic Surgery

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