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NCT06386250

Comparison of Regional Block, Caudal Block and Wound Infiltration in Inguinal Hernitomy

Comparison of Regional Block, Caudal Block and Wound Infiltration for Post-operative Pain Management in Children Undergoing Inguinal Herniotomy
King Edward Medical University·ClinicalTrials.gov·procedureCompleted
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Study focus
Disease/Condition
Postoperative Pain
Drug/Device/Intervention
regional block
Study type
Interventional
Intervention type
procedure
Sponsor & location
Primary sponsor
King Edward Medical University
Location
Lahore, Pakistan
Timeline & enrollment
Phase
N/A
Start date
Jan 05, 2019
End date
Jan 06, 2020
Enrollment
300 participants
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
Acute painPostoperative intestinal obstructionPain, unspecifiedDuring surgical operationDuring surgical operation
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06386250
Type
Non-Device Trial
About this record

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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