Comparison between propofol and dexamethasone for preventing postoperative nausea and vomiting after ENT surgeries.
Not yet recruiting
- Conditions
- Medical and Surgical,
- Registration Number
- CTRI/2022/10/046220
- Lead Sponsor
- Dr sathvika Pati
- Brief Summary
It is a randomized, prospective, comparative, double blinded, observational study where in intravenous propofol and intravenous dexamethasone are compared for preventing postoperative nausea and vomiting after ear, nose and throat surgery.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 60
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.
-
- Gastroesophageal reflux disease.
-
- Patients with known allergy to study drugs.
-
- 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. Immediate postoperative period, | After 30minutes, 1hour, 6hrs, 12hrs and 24hrs after giving study drug
- Secondary Outcome Measures
Name Time Method To observe any side effects First 24hrs postoperatively
Trial Locations
- Locations (1)
Dr. D.Y. Patil Medical College Hospital and Research Centre,Pimpri
🇮🇳Pune, MAHARASHTRA, India
Dr. D.Y. Patil Medical College Hospital and Research Centre,Pimpri🇮🇳Pune, MAHARASHTRA, IndiaDr Sathvika PatiPrincipal investigator7795446246sathvikareddy009@gmail.com