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To compare the pain reliving efficacy of two pain relieving medicines in postsurgery in pain patients coming for lower spine surgeries - due to spinal cord compressio

Not Applicable
Completed
Conditions
Health Condition 1: G55- Nerve root and plexus compressionsin diseases classified elsewhere
Registration Number
CTRI/2019/08/020573
Lead Sponsor
Institutional Review Board
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
50
Inclusion Criteria

1. ASA I AND II

2. Patients Undergoing Lumbar Laminectomy And Discectomy Surgery

3. Normal Renal Functions

Exclusion Criteria

1. ASA III OR IV

2. BMI >40

3. Impaired Renal Function

4. Intraoperative CSF Leak

5. Any Contraindications to Morphine and Ketamine

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Time Taken to Receive First Rescue AnalgesiaTimepoint: 3 Hours
Secondary Outcome Measures
NameTimeMethod
1. NRS score 1-10 <br/ ><br>2. Total Amount of Rescue Analgesic Consumed: Cumulative opioid Consumption <br/ ><br>3. Post OP Haemodynamics : HR , BP , RR , sedation <br/ ><br>4. Post OP Complications - Vomiting , Pruritis , urinary retention , Respiratory depression <br/ ><br>Timepoint: 24 Hours
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