Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Nil: Nil
Sponsors
Department of Anesthesiology
Eligibility
Inclusion criteria
Inclusion criteria: Patients of ASA 1-2 undergoing lowerlimb surgeries under spinal anaesthesia
Exclusion criteria
Exclusion criteria: Bleeding disorders Local skin infections Raised intracranial pressure Morbid obesity Height less than 150cm
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare Buprenorphine & Fentanyl when given intrathecally as an adjuvant to hyperbaric ropivacaine in terms of 1. Sensory blockade 2. Motor blockade 3. Incidence of bradycardia Incidence of hypotensionTimepoint: The sensory & motor block levels assessment was performed at 5 mins interval for the first 15mins then 15 mins interval for half an hour followed postoperative room (first one hour of shifting) | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare buprenorphine & fentanyl when given intrathecally as an adjuvant to hyperbaric ropivacaine in terms of 1. Incidence of nausea and vomiting 2. Incidence of pruritis and other side effectsTimepoint: Nausea, vomiting, post operative pain & pruritis will be assessed hourly in post operative unit upto 12 hours | — |
Countries
India
Contacts
Public ContactKaturi Srilakshmi
KS HEGDE MEDICAL ACADEMY
Outcome results
None listed