Health Condition 1: G952- Other and unspecified cord compression
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients willing to give written and informed consent Patients undergoing lumbar spine fixation surgery Patients with ASA physical status 1 or 2
Exclusion criteria
Exclusion criteria: Non cooperative patients BMI more than 35kg/m2 History of allergy to any other drugs used during the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To asses and compare mean NRS score at different intervals between the study groups To assess and compare in mean time of first rescue analgesia intravenous Diclofenac between the study groups To asses and compare the difference in mean total number of doses of intravenous Diclofenac in 24 hours postoperatively between the study groupsTimepoint: Just after extubation ,2hours ,6hours ,12hours, 24hours | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess and compare post operative hemodynamic vitals between the study groups To determine the proportion of patients experiencing side effects between study groupsTimepoint: Up to 24 hours of extubation | — |
Countries
India
Contacts
SMS medical college and hospital