Pain relief in spine surgeries.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: O- Medical and SurgicalHealth Condition 3: M518- Other thoracic, thoracolumbar andlumbosacral intervertebral disc disorders
- Registration Number
- CTRI/2021/12/038476
- Lead Sponsor
- Department of AnaesthesiaSNMedical College Intramural funds
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. ASA physical status 1 and 2.
2. Age 18-70 yrs.
3. Body mass index less than 30 kg/m2.
4. Patients undergoing elective lumbar spine surgeries.
Exclusion Criteria
1.Patient refusal to give consent
2.Co-morbidities like Anaemia , DM , HTN,
arthritis.
3.Moderate or severe renal impairment
( serum creatinine >=1.6 mg/dl)
4.Known asthmatic patient.
5.Opioids or other drug abuse.
6.Use of NSAIDs or Paracetamol in 24 hr
prior to surgery.
7.Participants with known allergy to study
groups
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pre - emptive combination of paracetamol-diclofenac, paracetamol-tramadol may reduce the total need for analgesic consumption and may prolong the time to first analgesia request when compared to paracetamol group.Timepoint: The NRS score will be recorded at recovery room when patient is fully awake from anaesthesia at 1,2,4,8,12 and 24 hrs. <br/ ><br>
- Secondary Outcome Measures
Name Time Method Pre-emptive combination of Paracetamol-Diclofenac and Pracetamol-Tramadol may reduce the total Tramadol consumption and prolongs the time to 1st analgesia request compared to Paracetamol alone. <br/ ><br>Timepoint: The NRS score will be recorded at recovery after the patient is fully awake from anaesthesia, at the end of 1,2,4,8,12 and 24 hr. <br/ ><br>