Comparison between propofol and dexamethasone for preventing postoperative nausea and vomiting after ENT surgeries.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/10/046220
- Lead Sponsor
- Dr sathvika Pati
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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
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
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the effect of propofol and dexamethasone for preventing postoperative nausea and vomiting.Timepoint: Immediate postoperative period, <br/ ><br>After 30minutes, 1hour, 6hrs, 12hrs and 24hrs after giving study drug
- Secondary Outcome Measures
Name Time Method To observe any side effectsTimepoint: First 24hrs postoperatively