Comparison of Regional Block, Caudal Block and Wound Infiltration in Inguinal Hernitomy - Trial NCT06386250
Access comprehensive clinical trial information for NCT06386250 through Pure Global AI's free database. This phase not specified trial is sponsored by King Edward Medical University and is currently Completed. The study focuses on Postoperative Pain. Target enrollment is 300 participants.
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Study Focus
Sponsor & Location
King Edward Medical University
Timeline & Enrollment
N/A
Jan 05, 2019
Jan 06, 2020
Primary Outcome
Postoperative pain intensity
Summary
Background: Although Inguinal herniotomy in children is taken as a day care procedure,
 post-operative pain management still remain controversial in these cases and superiority of
 wound infiltration, caudal block or regional block over each isn't known.
 
 Objective: The objective of the study was compare regional block, caudal block and wound
 infiltration for post-operative pain management in children undergoing inguinal herniotomy
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT06386250
Non-Device Trial