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Trial registered on ANZCTR
Registration number
ACTRN12616000957493
Ethics application status
Approved
Date submitted
4/07/2016
Date registered
20/07/2016
Date last updated
20/07/2016
Type of registration
Retrospectively registered
Titles & IDs
Public title
Effect of ondansetron on the duration of caudal block with bupivacaine on children who undergoing infraumbilical surgery
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Scientific title
Effect of intravenously administered ondansetron on the duration and level of caudal block on pediatric patients whom ondergoing infraumbilical surgery
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Secondary ID [1]
289598
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Nil known
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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:
infraumbilical pediatric surgery
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Condition category
Condition code
Anaesthesiology
299355
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0
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Pain management
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
intravenous 0.1 mg/kg ondansetron in 30 seconds will given pediatric patients whom undergo infraumbilical surgery before immediately prior to caudal block. Caudal block will performed regardless of enrolment in this trial.
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Intervention code [1]
295207
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Treatment: Drugs
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Comparator / control treatment
Control treatment is intravenous normal saline at the same volume.
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Control group
Placebo
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Outcomes
Primary outcome [1]
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caudal block duration time of analgesic effect will measured with faces pain scale
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Assessment method [1]
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Timepoint [1]
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postoperative 24 hour (1 time for every hour)
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Secondary outcome [1]
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caudal block sensorial level will tested with pin prick test.
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Assessment method [1]
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Timepoint [1]
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postoperative 8 hours ( 1 time for each hour)
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Eligibility
Key inclusion criteria
infraumbilical pediatric surgery patients and patients will be applied caudal block as part of the procedure
ASA ( American society of Anesthesiologists)physical status 1-2
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Minimum age
4
Years
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Maximum age
10
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
patients who dont want to participate
contrindication for caudal block application
BMI> 30 kg/m2
known allergic reactions to study drugs ( ondansetron, bupivacaine)
has neuorological or neuromuscular disease
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Study design
Purpose of the study
Treatment
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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)
central randomisation by computer
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people assessing the outcomes
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Intervention assignment
Parallel
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Other design features
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Phase
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
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Actual
10/06/2016
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Date of last participant enrolment
Anticipated
30/10/2016
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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
66
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
8002
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Turkey
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State/province [1]
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Konya
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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Baskent University
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Address [1]
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Baglica Kampusu Eskisehir Yolu 20. km Baglica
06810 ANKARA
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Country [1]
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Turkey
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Primary sponsor type
University
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Name
Baskent University
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Address
Baglica Kampusu Eskisehir Yolu 20. km Baglica
06810 ANKARA
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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]
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Baskent University Clinical Researches Ethical Committee
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Ethics committee address [1]
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Taskent Caddesi 77. Sokak No:11 06490 Bahcelievler Cankaya Ankara
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Ethics committee country [1]
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Turkey
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Date submitted for ethics approval [1]
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02/02/2016
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Approval date [1]
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29/04/2016
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Ethics approval number [1]
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KA 16/165
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Summary
Brief summary
Caudal epidural block is usually performing for pediatric patients whom underwent infraumbilical surgery. for postoperative analgesia. There are some publications showed that 5 HT-3 antagonist drugs like ondansetron, rapids sensorial block regression of neuroaxial anesthesia. We want to evaluate this effect on caudal block on pediatric patients. We include 4-10 years old ASA 1 or 2 patients who will undergo infraumbilical surgery. we will exclude if patients BMI is over 30 kg/m2, have neurological or neuromuscular disease, allergy to sudy drugs, have contrindication for caudal block. After routine monitorisation of patients and standart anesthetic induction for general anesthesia, we divide patients into two groups . We give 0.1 mg/kg ondansetron intravnously during seconds to Group Ondansetron and give same volume of serum physiologic for Group Control patients. After than we will perform caudal block with 1 ml/kg %0.025 bupivacaine at left decubitis position. After operation we will evaluate patients pain level with faces pain scale for 24 hours/ 1 time per hour and sensory level for 8 hours/ 1 time per hour. we will evaluate these findings and want to determine if there is a significant effect of ondansetron administration on the analgesic duration or sensorial level of caudal block.
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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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Mr Huseyin Ulas Pinar
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Address
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Baskent University,Hocacihan Mah. Saray Cad. No: 1 Selcuklu Postal Code: 42080
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Country
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Turkey
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Phone
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+903322570606
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Fax
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+903322570637
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Email
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[email protected]
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Contact person for public queries
Name
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Huseyin Ulas Pinar
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Address
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Baskent University Konya Research Center Anesthesiology Department,
Professional Address: Hocacihan Mah. Saray Cad. No: 1 Selcuklu/ Konya Postal Code: 42080
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Country
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Turkey
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Phone
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+903322570606
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Fax
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+903322570637
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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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Huseyin Ulas Pinar
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Address
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Baskent University Konya Research Center Anesthesiology Department,
Professional Address: Hocacihan Mah. Saray Cad. No: 1 Selcuklu/ Konya Postal Code: 42080
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Country
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Turkey
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Phone
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+903322570606
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Fax
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+903322570637
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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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