Health Condition 1: M498- Spondylopathy in diseases classified elsewhere
Conditions
Interventions
Intervention1: bilateral erector spinae block: Group B: patients will be receiving conventional general anaesthesia with bilateral ultrasound guided erector spinae block given with total volume of 40
Sponsors
pondicherry institute of medical sciences
Eligibility
Inclusion criteria
Inclusion criteria: 1)Age group of 18-65 yrs. 2)both genders 3)American society of anaesthesiologist: I /II 4)Patient undergoing primary open posterior spine fusion surgeries under general anaesthesia.
Exclusion criteria
Exclusion criteria: 1)patients BMI >35 2)History of Chronic opioid user 3)History of Patients with Coagulopathy 4)History of Patients with allergy to the study drug
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.To assess postoperative pain by using Visual analog score (VAS) for the first 24 hours between erector spinae plane block and conventional general anaesthesia groups in spine surgery patients.Timepoint: 24 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.To compare the hemodynamic parameters between erector spinae plane block and conventional general anaesthesia groups in spine surgery patients. 2.To determine the time for first opioid analgesia requirement in the postoperative period till 24 hours. 3.To determine the amount of cumulative opioid consumption between the groups during intraoperative and postoperative period till 24 hours. Timepoint: 1.To compare the hemodynamic parameters between erector spinae plane block and conventional general anaesthesia groups in spine surgery patients. 2.To determine the time for first opioid analgesia requirement in the postoperative period till 24 hours. 3.To determine the amount of cumulative opioid consumption between the groups during intraoperative and postoperative period till 24 hours. | — |
Countries
India
Contacts
Public ContactArish BT
pondicherry institute of medical sciences
Outcome results
None listed