Health Condition 1: R688- Other general symptoms and signs
Conditions
Interventions
Intervention1: preformed hyperbaric 0.5% levobupivacaine: we will administer this drug intrathecall for spinal anesthesia in patients posted for infraumblical surgeries
Control Intervention1: preforme
Sponsors
Mysore Medical College and research Institute
Eligibility
Inclusion criteria
Inclusion criteria: Americal society of anesthesiologist Grade 1 and 2 posted for infraumblical surgeries
Exclusion criteria
Exclusion criteria: patients allergic to drug raised intracranial pressure loacl site skin infections American society of Anesthesiologist grading 3 and 4
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of maximum sensory and motor blockade between hyperbaric bupivacaine 0.5% and levobupivacaine 0.5%. Assessment of haemodynamic stability with these both drugs Timepoint: baseline, 1 minute, 3 minutes, 10 minutes, 20 minutes, 30, 60, 90, 120, 180, 240 minutes, 6 hours, 12 hours, 24 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| Assessing of postoperative analgesia duration and time required for postoperative ambulationTimepoint: baseline, 60minutes, 90 minutes, 120 minutes, 180 minutes, 240 minutes, 6 hours, 12 hours, 24 hours | — |
Countries
India
Contacts
Public ContactDr Poolandevi K
Mysore Medical College and Research Institute
Outcome results
None listed