Health Condition 1: K819- Cholecystitis, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ASA Physical Status 1 and 2 Undergoing Elective Laparoscopic Surgeries
Exclusion criteria
Exclusion criteria: Patient Refusal Age less than 18 and more than 65 years ASA 3 and 4 Posted for Emergency Surgeries History of Allergy to Propofol and Dexmedetomidine Any Cardiovascular Disease including Severe Hypertension,Arrhythmias or Heart failure Liver or Renal Dysfunction Pregnant or Breast feeding Women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the efficacy of propofol infusion and dexmedetomidine infusion in maintaining an adequate depth of anaesthesia as measured by BIS Values during Laparoscopic surgeries and to evaluate the hemodynamic stability including Heart raye,Blood Pressure and Respiratory ParametersTimepoint: From 5 mins to 2 Hours Intraoperatively | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the recovery time,postoperative analgesic requirements and overall patient satisfaction after surgery to monitor adverse effects and complications associated with propofol and dexmedetomidine during anaesthesia maintainenceTimepoint: From 15 mins to 24 Hours Postoperatively | — |
Countries
India
Contacts
Vinayaka Missions Kirupananda Variyar Medical College and Hospitals Chinnaseeragapadi Salem