Health Condition 1: R688- Other general symptoms and signs
Conditions
Interventions
Intervention1: 0.75% ropivacaine.: 17ml of 0.75% ropivacaine through the epidural route
Control Intervention1: 0.5% levobupivacaine: 17ml of 0.5% levobupivacaine through the epidural route.
Sponsors
Saveetha medical college and hospital
Eligibility
Inclusion criteria
Inclusion criteria: Patients undergoing infra-umbilical surgeries Age 18 to 70 ASA I & II patients
Exclusion criteria
Exclusion criteria: Patient refusal Critically ill patients (ASA III & above) Patients with deformities of the spinal column Evidence of coagulopathy Infection at the site of the proposed epidural needle puncture Patients with mental disturbance or neurological disease Pregnant patients are excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| sensory & motor characteristics between 2 groups will be comparedTimepoint: sensory & motor characteristics between 2 groups will be compared | — |
Secondary
| Measure | Time frame |
|---|---|
| hemodynamic profile and complications between the two groups will be compared.Timepoint: Baseline hemodynamic parameters and hemodynamic profile at 0,2mins,5mins,10mins,15mins,20mins,25mins,30mins,1hour,1.5hours,2hours,2.5hours,3hours,3.5hoursand 4 hours will be compared | — |
Countries
India
Contacts
Public ContactThamizhmathi Thangaraju
Saveetha medical college and hospital.
Outcome results
None listed