Caudal Bupivacaine vs Bupivacaine Plus Two Doses of Dexmedetomidine for Postoperative Analgesia in Children
Information source: University of Jordan
ClinicalTrials.gov processed this data on August 20, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Pain, Postoperative
Intervention: Bupivacaine (Drug); dexmedetomidine 1μg.kg-1 (Drug); dexmedetomidine 2μg.kg-1 (Drug)
Phase: Phase 2/Phase 3
Status: Completed
Sponsored by: University of Jordan Official(s) and/or principal investigator(s): khaled R Al-zaben, Principal Investigator, Affiliation: University of Jordan Ibraheem Y Qudaisat, Study Director, Affiliation: University of Jordan
Summary
The aim of this prospective randomized double-blind study was to compare the analgesic
efficacy and the side effects of two doses of dexmedetomidine (1 and 2 µg. kg-1)
co-administered with bupivacaine with bupivacaine alone for caudal analgesia in children
undergoing infra-umbilical surgery.
Clinical Details
Official title: Comparison of Caudal Bupivacaine Alone With Bupivacaine Plus Two Doses of Dexmedetomidine for Postoperative Analgesia in Pediatric Patients Undergoing Infra-umbilical Surgery: A Randomized Controlled Double Blinded Study
Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Primary outcome: Time to first analgesic requirementPostoperative pain scores Number of postoperative analgesia doses
Secondary outcome: Postoperative sedation scoresSevoflurane concentration Blood pressure Heart Rate Side effects of study drugs
Detailed description:
- Quality assurance plan for data validation and registry: After Data was registered, it
was reviewed by a second person who compared it to the Data in patient data collection
forms.
- Data check: carried out using Statistical Package for the Social Sciences (SPSS)
variable definition protocols. Also data were entered in EXCEL sheets for comparisons
to guarantee consistency.
- Source data verification: Paper case report forms and medical records.
- Standard Operating Procedures to address registry operations and analysis activities:
Eligible patients were recruited after obtaining consent. Data was collected by
qualified personnel rained on the process. Data was entered into Excel sheets and SPSS
programs and compared for consistency. Analysis of Data was carried out by a qualified
statistician. Adverse events were reported as yes/no variables. Data of patients who
had Change in management was omitted from analysis.
- Sample size assessment: Sample size was calculated to detect a 65% reduction in the
analgesic requirement during the first 24 h from 75% in the bupivacaine group with α=
0. 05 and β=0. 80.
- Plan for missing data: Patients with missing Data were omitted from statistical
analysis.
- Statistical analysis plan: carried out using International Business Machines (IBM)
statistics 19. 0 statistical package for windows. Data were compared using analysis of
variance for continuous variables, Kruskal-Wallis test for ordinal, and chi square test
for categorical ones. Post hoc analyses were carried out as appropriate.
Eligibility
Minimum age: 1 Year.
Maximum age: 6 Years.
Gender(s): Both.
Criteria:
Inclusion criteria:
- Patients with American Society of Anesthesiologists (ASA) - I
- Scheduled for lower abdominal and perineal surgery
- Under general anesthesia
Exclusion criteria:
- history of developmental delay or mental retardation
- known or suspected coagulopathy or recent use of anticoagulant/antiplatelet drugs.
- known allergy to any of the study drugs.
- any signs of infection or congenital abnormalities at the site of the proposed caudal
block
Locations and Contacts
Additional Information
Related publications: Tong Y, Ren H, Ding X, Jin S, Chen Z, Li Q. Analgesic effect and adverse events of dexmedetomidine as additive for pediatric caudal anesthesia: a meta-analysis. Paediatr Anaesth. 2014 Dec;24(12):1224-30. doi: 10.1111/pan.12519. Epub 2014 Sep 9. Review. She YJ, Zhang ZY, Song XR. Caudal dexmedetomidine decreases the required concentration of levobupivacaine for caudal block in pediatric patients: a randomized trial. Paediatr Anaesth. 2013 Dec;23(12):1205-12. doi: 10.1111/pan.12278. Epub 2013 Oct 12. Bharti N, Praveen R, Bala I. A dose-response study of caudal dexmedetomidine with ropivacaine in pediatric day care patients undergoing lower abdominal and perineal surgeries: a randomized controlled trial. Paediatr Anaesth. 2014 Nov;24(11):1158-63. doi: 10.1111/pan.12478. Epub 2014 Jul 12. Saadawy I, Boker A, Elshahawy MA, Almazrooa A, Melibary S, Abdellatif AA, Afifi W. Effect of dexmedetomidine on the characteristics of bupivacaine in a caudal block in pediatrics. Acta Anaesthesiol Scand. 2009 Feb;53(2):251-6. doi: 10.1111/j.1399-6576.2008.01818.x. Epub 2008 Dec 6. El-Hennawy AM, Abd-Elwahab AM, Abd-Elmaksoud AM, El-Ozairy HS, Boulis SR. Addition of clonidine or dexmedetomidine to bupivacaine prolongs caudal analgesia in children. Br J Anaesth. 2009 Aug;103(2):268-74. doi: 10.1093/bja/aep159. Epub 2009 Jun 18. Findlow D, Aldridge LM, Doyle E. Comparison of caudal block using bupivacaine and ketamine with ilioinguinal nerve block for orchidopexy in children. Anaesthesia. 1997 Nov;52(11):1110-3. Xiang Q, Huang DY, Zhao YL, Wang GH, Liu YX, Zhong L, Luo T. Caudal dexmedetomidine combined with bupivacaine inhibit the response to hernial sac traction in children undergoing inguinal hernia repair. Br J Anaesth. 2013 Mar;110(3):420-4. doi: 10.1093/bja/aes385. Epub 2012 Nov 15. Konakci S, Adanir T, Yilmaz G, Rezanko T. The efficacy and neurotoxicity of dexmedetomidine administered via the epidural route. Eur J Anaesthesiol. 2008 May;25(5):403-9. Epub 2007 Dec 19. Wu HH, Wang HT, Jin JJ, Cui GB, Zhou KC, Chen Y, Chen GZ, Dong YL, Wang W. Does dexmedetomidine as a neuraxial adjuvant facilitate better anesthesia and analgesia? A systematic review and meta-analysis. PLoS One. 2014 Mar 26;9(3):e93114. doi: 10.1371/journal.pone.0093114. eCollection 2014. Review.
Starting date: January 2014
Last updated: March 10, 2015
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