Clinical Trials Directory

Trials / Completed

CompletedNCT06386250

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
300 (actual)
Sponsor
King Edward Medical University · Academic / Other
Sex
All
Age
3 Years – 12 Years
Healthy volunteers
Not accepted

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

Detailed description

Three hundred patients rom the department of pediatric surgery, KEMU/Mayo Hospital, were randomized in three study groups by a computer generated table. Regional block group (Group A), wound infiltration group (Group B), caudal block group (Group C). . Patients were assessed for postoperative pain intensity using FLACC pain scale at 0, 1, 2, 4, 8, 24 hours after surgery in children less than 8 years of age. Wong-Baker Faces pain Scale at 0, 1, 2, 4, 8, 24 hours after surgery in children more than 8 years of age. Patients were discharged after 24 hours. If pain score ≥ 4 was given intravenously, Ketoralac. Urinary retention was observed after 24 hours, wound infection was observed after 7 days.

Conditions

Interventions

TypeNameDescription
PROCEDUREregional blockIn group A, iliohypogastric and ilioinguinal nerves were blocked by using 0.25% bupivacaine 2ml/kg of combined with skin infiltration of adrenaline 1:200 000.
PROCEDURECaudal blockIn group B 0.25% bupivacaine 0.5ml/Kg was infiltrated at the surgical site.
PROCEDUREEpiduralIn group C 0.25% Bupivacaine 1ml /kg was given into epidural space at L4-L5 or L5-S1.

Timeline

Start date
2019-01-05
Primary completion
2020-01-06
Completion
2020-01-06
First posted
2024-04-26
Last updated
2024-04-26

Locations

1 site across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT06386250. Inclusion in this directory is not an endorsement.