RecruitingInterventionalNot ApplicableUpdated May 6, 2026
Effect of Dexmedetomidine on the Characteristics of High Volume/Low Concentration Ropivacaine in a Caudal Block in Pediatrics | NCT02163980 | Trialant
CompletedInterventionalNot ApplicableUpdated Jun 16, 2014
Effect of Dexmedetomidine on the Characteristics of High Volume/Low Concentration Ropivacaine in a Caudal Block in Pediatrics
ClinicalTrials.gov ID
NCT02163980
Lead Sponsor
Yonsei UniversityOTHER
Overall Status
Completed
Study Type
Interventional
Phase
Not Applicable
Enrollment
80Actual
Last Update Posted
Jun 16, 2014Estimated
Start Date
May 2011
Primary Completion Date
May 2011Actual
Completion Date
Jul 2011Actual
Brief Summary
The investigators perform this study to evaluate the effects of caudal Dexmedetomidine (DEX) added to high volume/low-concentration of ropivacaine in children undergoing orchiopexy.
Ambulatory Orchipexy
Caudal ropivacaine + normal saline
Caudal ropivacaine + dexmedetomidine
Ages Eligible for Study
Child (0-17)
Sexes Eligible for Study
Male
Accepts Healthy Volunteers
Yes
Eligibility Criteria
Inclusion Criteria:
children undergoing ambulatory orchiopexy,
ASA status I
Exclusion Criteria:
mental retardation,
developmental delay,
neurological or psychiatric illness,
coagulation disorder,
spinal anomalies
Primary Purpose
Prevention
Allocation
Randomized
Interventional Model
Parallel Assignment
Masking
Triple
No central contacts
There are no central contacts for this study.
Yonsei Univ. College of Medicine Dep. Of Anesthesiology