To compare the pain relief in spine surgery from two pain killer drugs (Bupivacaine and Morphine) delivered regionally around spinal cord using ultrasound guidance.
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Patients undergoing lumbosacralspine surgeries
- Registration Number
- CTRI/2017/11/010581
- Lead Sponsor
- AIIMS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
1. All patients, aged between 18-60 years, undergoing lumbosacral spine surgery ( trauma and degenerative) will be included in the study.
2. Patients willing to give consent .
Exclusion Criteria
1. Patient refusal
2. Patients with head injury or raised intracranial pressure.
3. Patents with coagulopathy.
4. Patients with infection at the local site.
5. Patients with allergy to the local anaesthetic drug.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.Time to first activation of PCA <br/ ><br>2.Total Morphine consumption <br/ ><br>3. VAS <br/ ><br>Timepoint: VAS â?? Immediate postoperative period, 2 hours, 4 hours, 6 hours, 12 hours and 24 hours <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1.Total intraoperative fentanyl requirement <br/ ><br>2. Incidence of Adverse effects. <br/ ><br>i.e. Respiratory depression <br/ ><br>Pruritus <br/ ><br>Nausea & vomiting <br/ ><br>Timepoint: 0(basal),5mins,10mins,15 mins, at SKIN INCISION,5 min ,10 min,15min,20 min,25 min,30 min, At INSTRUMENTATION,30 mins,60mins,90 mins <br/ ><br> <br/ ><br>