Ignite Creation Date:
2024-05-06 @ 8:26 PM
Last Modification Date:
2024-10-26 @ 3:28 PM
Study NCT ID:
NCT06386250
Status:
COMPLETED
Last Update Posted:
2024-04-26
First Post:
2024-04-13
Brief Title:
Comparison of Regional Block Caudal Block and Wound Infiltration in Inguinal Hernitomy
Sponsor:
King Edward Medical University
Organization:
King Edward Medical University
Study Overview
Official Title:
Comparison of Regional Block Caudal Block and Wound Infiltration for Post-operative Pain Management in Children Undergoing Inguinal Herniotomy
Status:
COMPLETED
Status Verified Date:
2024-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
Painseverity
Brief 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 isnt 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
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 KEMUMayo 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
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None