To compare two variety modes of pain decreasing methods on well being in patients undergoing backbone operation.
Not Applicable
Completed
- Conditions
- Health Condition 1: - Health Condition 2: G55- Nerve root and plexus compressionsin diseases classified elsewhere
- Registration Number
- CTRI/2019/12/022513
- Lead Sponsor
- Institutional Review Board
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
1.ASA grade I and II
2.Patients undergoing Transforaminal Lumbar Interbody fusion.
3.Normal renal function.
Exclusion Criteria
1.ASA III and IV
2.BMI >30
3. Impaired renal function.
4.Intraoperative csf leak
5.Previous surgical procedures in lumbo sacral region
6.Patients with psychiatric illness.
7.Obstructive sleep apnoea.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the Quality of recovery score between the two groups of patients using QoR 15 Score.Timepoint: Primary investigator will assess the Quality of recovery at the end of 48 hours after operation in the ward.
- Secondary Outcome Measures
Name Time Method 1. To compare the analgesic efficacy of the two techniques using Numeric rating scale at movement. <br/ ><br>2.Patient satisfaction score (0-10). <br/ ><br>3.Time of ambulation <br/ ><br>4.Length of hospital stay <br/ ><br>5. Sedation score, respiratory rate,Ponv,pruritus <br/ ><br>6.Time of receiving first rescue analgesia for breakthrough pain.Timepoint: 1. In the post anesthesia care unit by recovery staff at intervals of half an hour till discharge from recovery room <br/ ><br>. <br/ ><br> <br/ ><br>2 Post operative ward -.Pain nurse and ward staff will asess at the arrival to post operative ward, at 2 hrs, 6 hrs,12 hrs,24 hrs,36 hrs,48 hrs. <br/ ><br> <br/ ><br>3. Primary investigator will assess at end of 24 hrs and 48 hours after suggery. <br/ ><br>