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Comparison between propofol and dexamethasone for preventing postoperative nausea and vomiting after ENT surgeries.

To compare the effectiveness of propofol versus dexamethasone for preventing postoperative nausea and vomiting after ear, nose, and throat surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/10/046220
Enrollment
60
Registered
2022-10-06
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Control Intervention1: Intravenous dexamethasone 8mg single dose: Intravenous dexamethasone 8mg single dose given at the end of surgery for preventing postoperative nausea and vomiting Control Interve

Sponsors

Dr sathvika Pati
Lead Sponsor

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

MeasureTime 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

MeasureTime frame
To observe any side effectsTimepoint: First 24hrs postoperatively

Countries

India

Contacts

Public ContactDr Chhaya Suryawanshi

Dr. D. Y. Patil Medical College, Hospital & Research Centre

chhayasuryawanshi@gmail.com9922888201

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026