Health Condition 1: G890- Central pain syndrome
Conditions
Interventions
Intervention1: Group M: 2.8ml of 0.5%heavy bupivacaine with 100 mcg of morphine intrathecal
Intervention2: Group B: 2.8ml of 0.5% heavy bupivacaine with 60 mcg buprenorphine intrathecally
Control Inte
Sponsors
Sri Ramakrishna hospital
Eligibility
Inclusion criteria
Inclusion criteria: ASA Physical status 1 or 2 Presenting for infraumblical surgeries Patients who provide consent for the study
Exclusion criteria
Exclusion criteria: Patient allergic to the drug ASA Physical status 3 and above , acute or chronic respiratory disease, cognitive or psychiatric disturbances Any contraindication to subarachnoid block Pregnant women Day care procedures Patients who do not give consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the duration of postoperative analgesia of buprenorphine and morphine when given intrathecally with hyperbaric bupivacaineTimepoint: 2, 4, 8, 12, 24 hours of postoperative analgesia | — |
Secondary
| Measure | Time frame |
|---|---|
| Time taken to achieve maximum sensory and motor block Intraoperative hemodynamic changes like bradycardia and hypotension and intraoperative side effects like nausea, vomiting and pruritisTimepoint: Sensory and motor block will be assessed every 2 minutes till maximum level is reached | — |
Countries
India
Contacts
Public ContactHemamalini Arun
Sri Ramakrishna hospital , Coimbatore
Outcome results
None listed