Health Condition 1: null- Inhalational Agent consumption
Conditions
Interventions
Intervention1: Bupivacaine: Bupivacaine 0.25% given through continuous epidural infusion at 10ml/hour till the end of surgery
Control Intervention1: Normal Saline: Normal Saline 0.9% given through con
Sponsors
Mahatma Gandhi Medical College and Research Institute
Eligibility
Inclusion criteria
Inclusion criteria: Elective laparotomy, ASA I & II
Exclusion criteria
Exclusion criteria: History of substance abuse, major spine abnormalities, difficult airway, coagulation abnormalities and those on anti-convulsants or anti-depressants were excluded. Emergency laparotomies and patients with history of allergy to local anaesthetics
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percentage reduction of end tidal concentration of Sevoflurane when GA is combined with Epidural analgesiaTimepoint: Outcome assessed at the end of study | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare and quantify the difference in end tidal Sevoflurane requirement between the twoTimepoint: Assessed at the end of the study | — |
Countries
India
Contacts
Public ContactDalena Mathew
Mahatma Gandhi Medical College & Research Institute
Outcome results
None listed