Health Condition 1: K00-K95- Diseases of the digestive system Health Condition 2: K669- Disorder of peritoneum, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients belonging to ASA (American Society of Anesthesiologists) I and II consenting adult patients of either sex 2.patient aged between 18-70 years 3. patient weighing between 40-90kg.
Exclusion criteria
Exclusion criteria: 1. Patients with prior h/o neurologic, cardiopulmonary, liver or renal impairments and psychiatric disease 2. Pregnant women 3. Patients with coagulopathies and increased intracranial tension 4. Patient allergic to drugs used in the study 5. Having contraindications to epidural anesthesia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the efficacy of two local anesthetics as continuous epidural infusion for post operative pain analgesia in abdominal surgeries. Timepoint: baseline , 4weeks , 8 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare hemodynamic changes associated with two local anestheticsTimepoint: 0 mins , 30mins , 1st hour , 2nd hour , 4th hour , 8th hour , 16th hour , 24hours. | — |
Countries
India
Contacts
SDM MEDICAL COLLEGE AND HOSPITAL