Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patient willing to sign the written and informed consent. Age group: 18-70 years. Both male and female patients. Patients posted for laparoscopic cholecystectomy under general anaesthesia with ASA-1 or ASA-2 grade.
Exclusion criteria
Exclusion criteria: Patient s refusal from taking part in the study. Special populations. Pregnant and lactating women. History of allergy to drugs. Severe kidney and liver disease. Patients with neuropathies or nerve injuries. Patients with pain due to cause other than presenting disease.
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| To study any intraoperative complications like nausea, vomiting, rigors, bradycardia, respiratory depression, hypotension.Timepoint: Hemodynamic parameters will be recorded at 2 minutes 5 minutes 10 minutes 20 minutes 30 minutes 45 minutes 60 minutes 75 minutes 90 minutes 105 minutes 120 minutes | — |
Primary
| Measure | Time frame |
|---|---|
| To compare the analgesic effect and safety profile of intravenous paracetamol v/s intravenous diclofenac in post-operative pain management in laparoscopic cholecystectomy surgeries. Timepoint: To study analgesic efficacy of intravenous paracetamol and intravenous diclofenac as post-operative pain management in laparoscopic cholecystectomy post-operatively at 30 minutes,4 hours, 8 hours, 12 hours, 24 hours. | — |
Countries
India
Contacts
Smt.Bhikiben Kanjibhai Shah Medical Institute and Research Centre