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Effect of ondansetron on the duration of caudal block with bupivacaine on children who undergoing infraumbilical surgery

Effect of intravenously administered ondansetron on the duration and level of caudal block on pediatric patients whom ondergoing infraumbilical surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12616000957493
Enrollment
66
Registered
2016-07-20
Start date
2016-06-10
Completion date
2016-10-30
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

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.

Interventions

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.

Sponsors

Baskent University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
4 Years to 10 Years
Healthy volunteers
No

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

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

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026