Transversus Abdominis Plane Block and Quadratus Lumborum Block in Pediatric Patients
Primary Purpose
Pain, Postoperative
Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Tramadol hydrochloride
Sponsored by
About this trial
This is an interventional other trial for Pain, Postoperative focused on measuring quadratus lumborum block, pediatric anesthesia, transverse abdominal block
Eligibility Criteria
Inclusion Criteria:
- The study included 40 cases undergoing lower abdominal surgery aged from 3 to 16 years with American Society of Anesthesiologist I-II level.
Exclusion Criteria:
- Cases with American Society of Anesthesiologist III-IV health level and those with a history of allergy to local anesthetic medications were not included in the study
Sites / Locations
- Döndü Genç Moralar
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
TAP Block
QL Block
Arm Description
Cases were assessed transversus abdominis plane block for postoperative analgesia
Cases were assessed quadratus lumborum block for postoperative analgesia
Outcomes
Primary Outcome Measures
the analgesic use of the groups in 24 hours
the number of analgesic requirements
Secondary Outcome Measures
Full Information
NCT ID
NCT04209478
First Posted
December 20, 2019
Last Updated
January 10, 2020
Sponsor
Bakirkoy Dr. Sadi Konuk Research and Training Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04209478
Brief Title
Transversus Abdominis Plane Block and Quadratus Lumborum Block in Pediatric Patients
Official Title
Transversus Abdominis Plane Block Versus Quadratus Lumborum Block for Postoperative Analgesia in Pediatric Patients; a Prospective, Randomized, Controlled Study
Study Type
Interventional
2. Study Status
Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
May 1, 2016 (Actual)
Primary Completion Date
November 30, 2016 (Actual)
Study Completion Date
November 30, 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Bakirkoy Dr. Sadi Konuk Research and Training Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
In the pediatric age group, postoperative pain is very important for the children to have a comfortable and problem-free postoperative period.
In the present study, it was aimed to compare the postoperative analgesic efficacy of Transversus abdominis plane (TAP) Block, and quadratus lumborum block (QLB) Type 1 on the pediatric patients
Detailed Description
Patients included in the study were randomly divided into 2 groups. Cases were assessed ultrasonography-guided TAP block (Group B, n=20) or ultrasonography-guided QL Block. Total analgesic amounts in 24 hours and first analgesic requirement times recorded.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pain, Postoperative
Keywords
quadratus lumborum block, pediatric anesthesia, transverse abdominal block
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Arm Title
TAP Block
Arm Type
Experimental
Arm Description
Cases were assessed transversus abdominis plane block for postoperative analgesia
Arm Title
QL Block
Arm Type
Experimental
Arm Description
Cases were assessed quadratus lumborum block for postoperative analgesia
Intervention Type
Drug
Intervention Name(s)
Tramadol hydrochloride
Other Intervention Name(s)
morphine hydrochloride
Intervention Description
The Wong-Baker facial pain scale was used to assess pain (1: no pain, 10: worst possible pain). During monitoring patients with pain score ≥3 had intravenous 1 mg/kg tramadol hydrochloride administered, After 15 minutes following tramadol injection, cases with pain score continuing ≥3 were to be assessed as insufficient analgesia and had 0.1 mg/kg morphine hydrochloride planned for intravenous administration
Primary Outcome Measure Information:
Title
the analgesic use of the groups in 24 hours
Description
the number of analgesic requirements
Time Frame
how many times in 24 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
The study included 40 cases undergoing lower abdominal surgery aged from 3 to 16 years with American Society of Anesthesiologist I-II level.
Exclusion Criteria:
Cases with American Society of Anesthesiologist III-IV health level and those with a history of allergy to local anesthetic medications were not included in the study
Facility Information:
Facility Name
Döndü Genç Moralar
City
Istanbul
ZIP/Postal Code
34000
Country
Turkey
12. IPD Sharing Statement
Plan to Share IPD
No
Links:
URL
https://www.ncbi.nlm.nih.gov/pubmed/?term=Blanco+R%2C+Ansari+T%2C+Riad+W%2C+Shetty+N.+Quadratus+Lumborum+Block+Versus+Transversus+Abdominis+Plane+Block+for+Postoperative+Pain+After+Cesarean+Delivery.
Description
Related Info
Learn more about this trial
Transversus Abdominis Plane Block and Quadratus Lumborum Block in Pediatric Patients
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