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Comparison between two methods of pain relief after Hernia surgery in children.

Completed
Conditions
undergoing unilateral inguinal herniotomy for circumscision, congential hernia
Registration Number
CTRI/2017/04/008341
Lead Sponsor
Mahatma Gandhi Memorial Government Hospital
Brief Summary

To evaluate the efficacy of the Ultrasound-guidedTransversus Abdominis Plane Block in comparison with the Caudal Epidural Block,for pain relief in paediatric inguinal hernia repair surgeries

**Methodology:**

Sixty patients belonging to the age group 1-7years, weighing 5-20kgundergoing unilateral inguinal herniotomy were randomly allocated into twogroups. Group T (n=30) received USG-guided TAP block with 0.5ml/kg of 0.25%bupivacaine and Group C (n=30) received 1ml/kg of 0.25% bupivacaine, afterinstitution of general anaesthesia via ambu LMA. The intra-operativehemodynamics and analgesic requirement were recorded by a blinded investigator.Pain  in the post-operative period wasassessed using FLACC pain score. Time to first rescue analgesia, cumulativeopioid consumption, along with the incidence of side effects were noted in thefirst 12hrs of the post-operative period

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Children weighing 5-20kg 2.
  • Children belonging to ASA Physical status I & II 3.
  • Children undergoing elective inguinal herniotomy 4.
  • Children undergoing unilateral surgery.
Exclusion Criteria
  • Children undergoing bilateral Inguinal Herniotomy 2.
  • children belonging to ASA status III, IV, 3.
  • Children of age less than 2yrs or more than 7yrs, excluded 4.
  • Children weighing less than 5 kg or more than 20kg 5.
  • Children with known allergy to the drugs used in the study 6.
  • Children with any contraindications for caudal anaesthesia such as major sacral malformations, meningitis, raised intracranial hypertension 8.
  • Parent refusal for consent were excluded from the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain assessment in the post-operative period was done using FLACC pain score.Children were monitored during the time points; | 1. immediate post-operative period in the recovery room | 2. every hour for the first 12hrs in the post-operative period
Secondary Outcome Measures
NameTimeMethod
•Intraoperative parameters measured:1.Haemodynamic variability

Trial Locations

Locations (1)

Mahatma Gandhi Memorial Government Hospital, Thillai Nagar, Puthur, Trichy- 620017

🇮🇳

Tiruchirappalli, TAMIL NADU, India

Mahatma Gandhi Memorial Government Hospital, Thillai Nagar, Puthur, Trichy- 620017
🇮🇳Tiruchirappalli, TAMIL NADU, India
Dr Selvakumar R
Principal investigator
9842165067
drselvakumar@rediffmail.com

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