Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) ASA grade I – II patients 2) Aged 18 – 65 years 3) Patients willing to participate 4) Patients undergoing lumbar laminectomies and discectomies.
Exclusion criteria
Exclusion criteria: 1) Patient who refused to participate 2) Morbidly obese patients 3) Pregnancy 4) Severe hepatic insufficiency 5) Severe renal insufficiency 6) Spinal deformities 7) Drug allergies used in the study 8) Cardiac or respiratory compromise 9) Coagulation profile abnormalities 10) Patients on beta blockers 11) Patients with neurological deficit
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1) Duration of analgesia ( after giving block)initial use of rescue analgesia for surgical site painTimepoint: 1) Duration of analgesia 6hr to 8hr ,12hrs,16hrs till 48hrs after giving block)initial use of rescue analgesia for surgical site pain( if patient complains of pain inj .ketrolac should be given)pain initial use of rescue analgesia for surgical site pain | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) To evaluate the efficacy of levobupivacaine with dexmedetomidine and bupivacaine with dexmedetomidine in terms of maximum visual analogue scale (VAS) pain score and consumption of rescue analgesia. 2) To assess time for mobilization for the patients undergoing lumbar laminectomies. 3) Comparison of intraoperative hemodynamics between two groups. 4) Comparison of readiness for discharge in the two groups.Timepoint: VISUAL ANALOGUE SCALE | — |
Countries
India
Contacts
nizams institute of medical sciences,panjagutta hyderabad