Comparing Levobupivacaine 0.25% and Ropivacaine 0.25% for caudal epidural anaesthesia for infra umbilical surgeries in childre

Phase 3

• Conditions: Health Condition 1: O- Medical and Surgical

• Registration Number: CTRI/2024/03/064524
• Lead Sponsor: Dr Manchikanti V D Avinash

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 1 April 2024

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1.ASA 1 AND 2

2.Patients undergoing elective infraumbilical surgeries

3.Parental consent

4.Duration of surgery less than 1 hour

Exclusion Criteria

1.Patients who are allergic to local anaesthetics

2. Patients with coagulation abnormalities

3.Patients with spinal abnormalities and neurological deficits.

4. Patients with infection at the site of block

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To evaluate the effectiveness of analgesia and drug with less toxic effect of 0.25% Levobupivacaine and 0.25% Ropivacaine in Paediatric patients undergoing infra umbilical surgeries under caudal epidural anaesthesia.Timepoint: 5,10,15,20,25,30,35,40,45,50,55 and 60 minutes

Secondary Outcome Measures

Name	Time	Method
Duration of post operative analgesia and complications if anyTimepoint: 5,10,15,20,25,30,35,40,45,50,55 and 60 minutes