None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Belonging to ASA grade2 2.Patients receiving spinal anaesthesia with either ropivacaine or bupivacaine 3.Willing to give informed and verbal consent to participate in the study
Exclusion criteria
Exclusion criteria: 1 Patients contraindicated for spinal anaesthesia 2 Gestational diabetes mellitus 3 Cardiac disorders 4 Fetal distress 5 Pregnancy induced hypertension 6 Cord prolapse 7 Placenta previa 8 Antepartum hemorrhage
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate and compare analgesic effect of hyperbaric ropivacaine and hyperbaric bupivacaine for regression to L5 levelTimepoint: 300mins | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.To study the onset and duration of motor block of hyperbaric ropivacaine and hyperbaric bupivacaine 2. To study the variations in hemodynamic parametersTimepoint: 300mins | — |
Countries
India
Contacts
Pravara institute of medical sciences, Loni