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
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