A clinical trial to study if adding adjuvant to local anesthetic in Erector spinae block for post operative pain relief in lower spine surgery is beneficial.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/01/039361
- Lead Sponsor
- Dr Vinod C
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA Physical status 1 and 2.
Patients posted for elective lumbar spine surgery.
Exclusion Criteria
Patients allergic to local anesthetics.
Patients with severe cardiovascular, renal, respiratory and endocrinal disorders.
Patients with coagulation disorder.
Pregnancy and Lactation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Post operative analgesia.Timepoint: 2hr, 4hr, 6hr, 8hr
- Secondary Outcome Measures
Name Time Method Effect of addition of Dexamethasone to Bupivacaine.Timepoint: 2hr, 4hr, 6hr, 8hr