Health Condition 1: 4- Measurement and Monitoring
Conditions
Interventions
Intervention1: Hyperbaric Ropivacaine 0.75% in Spinal Anaesthesia: Dose - 3cc of 0.75% Hyperbaric Ropivacaine
Route of Administration - Subarachnoid Space
Control Intervention1: Hyperbaric Levobupi
Sponsors
D Y Patil University School of Medicine and Hospital Nerul Navi Mumbai
Eligibility
Inclusion criteria
Inclusion criteria: Patient undergoing various infra-umbilical surgeries under spinal anaesthesia ,Asa grade 1 and 2, Age 18-60 years
Exclusion criteria
Exclusion criteria: Refusal ofspinal anaesthesia Asa grade 3 and 4 Head injury and raised ICP Psychiatric diseases Known allergy to test drug Infection at site of injection Uncontrolled hypovolemia Coagulopathies Fixed cardiac output ststes
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the efficacy of Ropivacaine and Levobupivacaine based on : a)Onset and duration of sensory blockade b)Onset and duration of motor blockade Timepoint: To compare the efficacy of Ropivacaine and Levobupivacaine based on : a)Onset and duration of sensory blockade b)Onset and duration of motor blockade | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare in the two groups: 1)Maximum height of sensory blockade, 2) Hemodynamic effects 3)Complications or side effects if any . Timepoint: In 3 hours | — |
Countries
India
Contacts
Public ContactDR ANURADHA MALLIWAL
DR D Y PATIL UNIVERSITY AND SCHOOL OF MEDICINE
Outcome results
None listed