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Trial registered on ANZCTR
Registration number
ACTRN12611000585921
Ethics application status
Approved
Date submitted
2/06/2011
Date registered
7/06/2011
Date last updated
14/06/2011
Type of registration
Retrospectively registered
Titles & IDs
Public title
Ultrasound-Guided Transversus Abdominis Plane Block in Pediatric Patients: A Randomized Controlled Study
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Scientific title
The analgesic efficacy of the ultrasound-guided transversus abdominis plane block with high volume local anesthetic during the first 24 hours after surgery in pediatric patients undergoing inguinal hernia repair.
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Secondary ID [1]
262303
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Nil
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
inguinal hernia in pediatrics
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postoperative analgesia
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Condition category
Condition code
Anaesthesiology
268143
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0
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Anaesthetics
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
For postoperative analgesia ultrasound guided unilateral transversus abdominis plane block was applied with 0.5 mL/kg 0.25 % levobupivacaine just before surgical incision for inguinal hernia repair only one time.
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Intervention code [1]
266696
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Treatment: Drugs
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Comparator / control treatment
Infiltration anesthesia with 0.2 mL/kg 0.25 % levobupivacaine for postoperative analgesia just after unilateral inguinal hernia repair
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Control group
Active
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Outcomes
Primary outcome [1]
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First analgesic requirement time by using clinical assessments including pain scoring system
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Assessment method [1]
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Timepoint [1]
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Postoperative first 24 hours
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Secondary outcome [1]
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The cumulative number of uses of analgesic by using clinical assessments
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Assessment method [1]
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Timepoint [1]
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Postoperative first 24 hours
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Secondary outcome [2]
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pain scores by using clinical assessments
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Assessment method [2]
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Timepoint [2]
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Postoperative first 24 hours
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Eligibility
Key inclusion criteria
American Society of Anesthesiologist (ASA) class I-II children between 2 and 8 years of age, who were scheduled for unilateral inguinal hernia repair
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Minimum age
2
Years
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Maximum age
8
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Psychiatric illness, kidney failure and known hypersensitivity to relevant drugs.
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Study design
Purpose of the study
Prevention
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
Phase 4
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
20/12/2010
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
60
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
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Turkey
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State/province [1]
3611
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Funding & Sponsors
Funding source category [1]
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Hospital
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Name [1]
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Hospital of Gaziantep University
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Address [1]
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University st. 27310 Sehitkamil Gaziantep
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Country [1]
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Turkey
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Primary sponsor type
Individual
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Name
Levent Sahin
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Address
University st. 27310 Sehitkamil Gaziantep
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Country
Turkey
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
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Country [1]
266255
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Ethical Committee of Gaziantep University Hospitals
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Ethics committee address [1]
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Gaziantep University, University st. 27310, Sehitkamil, GAziantep
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Ethics committee country [1]
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Turkey
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Date submitted for ethics approval [1]
269177
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Approval date [1]
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16/12/2010
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Ethics approval number [1]
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4/12/2010
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Summary
Brief summary
The present study was designed to evaluate the analgesic efficacy of ultrasound-guided transversus abdominis plane block with high volume local anesthetic during the first 24 hours after surgery in pediatric patients undergoing inguinal hernia repair. Fifty seven children between 2 to 8 years of age undergoing unilateral inguinal hernioraphy were randomized to undergo a transversus abdominis plane block or to the infiltration anesthesia as control group. Intervention(s): A TAP block was performed using the ultrasound-guided technique with 0.5 mL/kg 0.25 % levobupivacaine volume on the ipsilateral side to the hernia under general anesthesia. Main outcome measures: First analgesic requirement time, cumulative number of uses of analgesic, pain scores and adverse effects were assessed over the course of 24 hours.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Levent Sahin
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Address
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Gaziantep University, University st. 27310, SEhitkamil Gaziantep
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Country
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Turkey
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Phone
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00 90 342 3606060 # 77804
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Levent Sahin
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Address
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Gaziantep University, University st. 27310, SEhitkamil Gaziantep
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Country
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Turkey
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Phone
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00 90 342 3606060 # 77804
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Fax
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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