Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Ropivacaine with dexamethasone: Ropivacaine 3 mg/kg body weight + 8 mg dexamethasone diluted in 100ml normal saline
instilled intraperitoneally once through veress needle before creatio
Sponsors
Dr Soumya Patted
Eligibility
Inclusion criteria
Inclusion criteria: Patients giving informed written consent Patients age between 18 – 60 years Patients scheduled for elective laparoscopic cholecystectomy under general anaesthesia Patients belonging to ASA I, II
Exclusion criteria
Exclusion criteria: Patients who refused to give informed written consent. Patients with ASA physical status III or more. Patients posted for emergency surgeries. Patients with history of alcohol or drug abuse. Patients who have allergy or hypersensitivity to local anaesthetics Pregnant or breastfeeding women. Patients with mental illness. Patients of renal,pulmonary, cardiovascular, hepatic, neurological, neuromuscular diseases Patients with anticipated difficult intubation Patients with acute cholecystitis, acute pancreatitis or peritonitis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the pre-emptive analgesia with intraperitoneal instillation of ropivacaine with dexamethasone versus ropivacaine alone versus normal saline Timepoint: Immediate post operative period then 1,3,6,12,24 hours in post operative period | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the hemodynamic parameters like blood pressure,heart rate, oxygen saturation etc and adverse effects with intraperitoneal instillation of ropivacaine with dexamethasone versus ropivacaine alone versus normal salineTimepoint: Baseline value,after intubation, before and after port insertion then every 5 minutes for first 30 minutes later every half an hour till end of surgery.1,3,6,12,24 hours in post operative period | — |
Countries
India
Contacts
Public ContactDr Samudyatha T J
Bangalore Medical College and Research Institute
Outcome results
None listed