Health Condition 1: null- American Society of Anapatientsesthesiologists Class I and II
Conditions
Interventions
Intervention1: Group A: (MMA group/study group): Received intravenous diclofenac sodium 75mg, paracetamol 1gm, and clonidine 0.75µg/kg, and local infiltration 20ml (bupivacaine 0.25% with adrenalin
Sponsors
Dr Savitha K S
Eligibility
Inclusion criteria
Inclusion criteria: 1. Both sexes 2. BMI (Body Mass Index) 18 to 30 3. Patients undergoing lumbar spine surgery 4. ASA physical status I and II
Exclusion criteria
Exclusion criteria: 1. Pregnant women 2. Patients with bronchial asthma 3. Patients with history of drug allergy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the difference in serum cortisol and random blood sugar between MMA regime and the conventional analgesic regime in patients undergoing lumbar spine surgery.Timepoint: Two blood samples were drawn; one just before tracheal tube placement and another one 30 min following skin incision for random serum cortisol and random blood sugar. | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare post extubation sedation and visual analogue score (VAS) between the two groups.Timepoint: Post operative sedation and pain score were assessed at 5min and 30min post-extubation respectively.;To compare the incidence of adverse effects (perioperatively:bradicardia and bronchospasm, postoperatively: respiratory depression, nausea and vomiting ) between the two groups.Timepoint: Bradicardia and bronchospasm were looked after administration of of each drug preoperatively and throught the surgery. Respiratory depression, nausea and vomiting were looked for in the postoperative period | — |
Countries
India
Contacts
Public ContactDr Savitha K S
St Johns Medical College & Hospital
Outcome results
None listed