Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients in age group of 18 to 60 years Patients with ASA I and II Hemodynamic stable patients Patients posted for ear, nose and throat surgery under general anaesthesia Patients willing to give consent to participate in the study.
Exclusion criteria
Exclusion criteria: Patients with previous history of nausea or vomiting. 2) Gastroesophageal reflux disease. 3) Patients with known allergy to study drugs. 4) Obese patient 5) Patients with ASA >II 6) Lack of patient consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the effect of propofol and dexamethasone for preventing postoperative nausea and vomiting.Timepoint: Immediate postoperative period, After 30minutes, 1hour, 6hrs, 12hrs and 24hrs after giving study drug | — |
Secondary
| Measure | Time frame |
|---|---|
| To observe any side effectsTimepoint: First 24hrs postoperatively | — |
Countries
India
Contacts
Dr. D. Y. Patil Medical College, Hospital & Research Centre