Efficacy of Intravenous Dexamethasone on Postoperative Caudal Analgesia in Pediatric Orchiopexy
Not Applicable
Completed
- Conditions
- Pain
- Registration Number
- NCT01041378
- Lead Sponsor
- Yonsei University
- Brief Summary
The purpose of this study is to evaluate postoperative pain control for pediatric patients.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
- Pediatric patients scheduled for elective day-case orchiopexy.
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Exclusion Criteria
- Infants or children with history of steroid allergy, renal, hepatic disease, or contraindication for caudal analgesia.
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Children's Hospital of Eastern Ontario Pain Scale, CHEOPS and Faces, Legs, Activity, Cry, and Consolability, FLACC postoperative 24 hours
- Secondary Outcome Measures
Name Time Method