Comparison of perioperative analgesia in patients undergoing lumbar spine surgery
Not Applicable
- Conditions
- Health Condition 1: G541- Lumbosacral plexus disorders
- Registration Number
- CTRI/2023/09/057847
- Lead Sponsor
- Department of Neurosurgery
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patient of either sex, Age group of20-65years
ASA I or II
Lumbar spine surgery
Exclusion Criteria
Patient Refusal
Coagulation disorders
Allergies to morphine or study drugs
Revision lumbar surgeries
Severe respiratory illness (COPD, OSA)
Psychiatric illness
Pregnancy or Lactation
Chronic opioid or analgesic use/abuse
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method oTo compare the analgesia using numeric rating scale (NRS) in intrathecal morphine vs erector spine plane block for perioperative analgesiain patient undergoing lumbar spine surgery.Timepoint: 24 to 48hrs
- Secondary Outcome Measures
Name Time Method oTo compare the sedation score <br/ ><br>oTo compare the patient satisfaction score <br/ ><br>oTo compare the consumption of rescue analgesic <br/ ><br>oTo compare the hemodynamic (HR, SBP, DBP, MAP, RR, SpO2) <br/ ><br>oTo study the complications (PONV, Respiratory depression, Bradycardia, Pruritus) <br/ ><br>Timepoint: 48hrs