Comparison of pain relief offered by two different techniques in the postoperative period in patients undergoing multilevel spinal surgery
Phase 3
Completed
- Conditions
- Health Condition 1: M480- Spinal stenosis
- Registration Number
- CTRI/2021/07/034956
- Lead Sponsor
- Association of Spine Surgeons of India
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
Multilevel Lumbar decompression
ASA grade 1,2
Exclusion Criteria
Revision surgery, Age >70
Lumbar fusion
Trauma, Infection, Tumor leading to single level fusions
Renal impairment
Allergy to NSAIDS, Pregabalin
Liver disease
Previous stroke, Myocardial infarction
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. 24-hour fentanyl consumption <br/ ><br> <br/ ><br>2. Visual Analogue score(VAS) <br/ ><br> <br/ ><br>3.Numeric rate scale (NRS) scoreTimepoint: 1. 24-hour fentanyl consumption measured using PCA pumps <br/ ><br> <br/ ><br>2. Visual Analogue score(VAS) post op 4hr,8hr,12hr,24hr,48hr,72hr,at Discharge and end of 4 week. <br/ ><br> <br/ ><br>3.Numeric rate scale (NRS) score In bed day1, In bed Day2, ambulation Day 1 and Ambulation Day 2
- Secondary Outcome Measures
Name Time Method 1. Reported Adverse events and Reactions. (Vomiting/Ileus/Sedation Score/Respiratory Depression/ Hypotension)Timepoint: Anytime during the study period