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NCT05969613 Clinical Trial

Comparison of Regional Block, Wound Infiltration and Caudal Block for Pain Management in Children

Inguinal Hernia Clinical Trial

— RCT  

Official title:
Comparison of Regional Block, Wound Infiltration and Caudal Block for Post Operative Pain Management in Children Undergoing Inguinal Herniotomy

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05969613
Other study ID # Fnaumeri
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2019
Est. completion date June 1, 2020

Study information
Verified date July 2023
Source King Edward Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Comparison of regional block, wound infiltration and caudal block for post operative pain management in participants undergoing inguinal herniotomy.

Description:

Investigators are comparing three modalities (regional block, wound infiltration and caudal block), for post operative pain management in participants after inguinal herniotomy.

Recruitment information / eligibility
Status Completed
Enrollment 2
Est. completion date June 1, 2020
Est. primary completion date October 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 2 Months to 12 Years
Eligibility Inclusion Criteria: 1. •Patients under 13 years of age 2. •Inguinal hernia Exclusion Criteria: 1. •History of allergy to any drugs used in study documented on history. 2. •Infection at the site of regional, caudal or local infiltration, documented on clinical examination. 3. •Irreducible, obstructed or strangulated hernia, documented on clinical examination.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Regional block
regional block with 0.25% Bupivacaine at a dose of 2ml/kg with adrenaline
• Wound infiltration
Infiltration of surgical site with 0.25% Bupivacaine at 0.5ml/kg dose
• Caudal block
Infiltration of caudal epidural space with 0.25% Bupivacaine at 1ml/kg dose

Locations
Country Name City State
Pakistan Mayo Hospital Lahore Punjab

Sponsors (1)
Lead Sponsor Collaborator
King Edward Medical University

Country where clinical trial is conducted

Pakistan, 

Outcome
Type Measure Description Time frame Safety issue
Primary post operative pain -FLACC Pain sacle Post operative pain management will be calculated by use of FLACC Pain scale . An overall pain score ranging from 0 to 10. Within 24 hours
Primary post operative pain -Wong-Baker Faces pain scale The scale shows a series of faces ranging from a happy face at 0, or "no hurt", to a crying face at 10, which represents "hurts like the worst pain imaginable". Within 24 hours
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