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

Recruiting

• Conditions: infraumbilical pediatric surgery; Anaesthesiology - Pain management

• Registration Number: ACTRN12616000957493
• Lead Sponsor: Baskent University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-07-20
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 66

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

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
caudal block duration time of analgesic effect will measured with faces pain scale [postoperative 24 hour (1 time for every hour)]

Secondary Outcome Measures

Name	Time	Method
caudal block sensorial level will tested with pin prick test.[postoperative 8 hours ( 1 time for each hour)]