Study to compare between Levobupivacaine and Ropivacaine in infra-umbilical surgeries for epidural anaesthesia
Phase 4
- Registration Number
- CTRI/2023/06/054380
- Lead Sponsor
- Dr Shreya Putta
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients undergoing a given Infra umbilical surgeries giving consent to participate in study. Age between 18 to 60 years. ASA grade I and grade II
Exclusion Criteria
Patients not giving consent to participate in the study.
ASA grade III and IV
Patients with respiratory, cardiovascular, hepatic and renal diseases, obesity.
Age below <18 years and above >60 years.
Any bleeding disorder and patient on anticoagulants.
Neurological and musculoskeletal disease.
Local infection at the injection site.
History of hypersensitivity or allergy to any drug
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Expected early onset of sensory & motor blockade & prolonged duration of analgesia with epidural ropivacaine 0.75%Timepoint: 24 hours
- Secondary Outcome Measures
Name Time Method Expected stable haemodynamic profile & lesser side effects with epidural levobupivacaine 0.5%Timepoint: 24 hours