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Assessment of pain relief in children undergoing hernia surgeries with multiple pain relieving methods using a apin monitor.

Not Applicable
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2022/03/040794
Lead Sponsor
Rajarajeswari Medical College and Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Children belonging to ASA physical status I aged between 3-8 years.

2.Elective herniotomy

Exclusion Criteria

1.Children requiring ketamine, glycopyrrolate, atropine, muscle relaxants, reversal agents

2. Children with fever and recent upper respiratory tract infection

3.Children with cardiac dysrhythmias, neurological diseases, renal, hepatic disease

4.Children with contraindications to regional analgesia (Caudal)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Primary outcome is adequacy of intraoperative analgesia which is measured by Analgesia Nociceptive index (values between 50 to70 denotes adequate analgesia) <br/ ><br>Timepoint: Measured every 5 minutes till the end of surgery. <br/ ><br> <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
1.To evaluate the clinical performance of Analgesia nociceptive Index in the assessment of immediate postoperative analgesia in pediatric patients who have undergone hernia surgeries under general anaesthesia.Timepoint: intaoperative and immediate post operative period for 2 hours
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