STUDY COMPARING ONDANSETRON AND PALONOSETRON IN REDUCING VOMITING IN PATIENTS AFTER ENT SURGERIES
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/03/063674
- Lead Sponsor
- DR SOMSUNDAR R G
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Aged between 18 to 60 years
2.ASA I and II category patients
3.Patients undergoing elective otorhinolaryngology surgeries under general anaesthesia
4.Patients willing to give informed consent to participate in the study.
Exclusion Criteria
1.Allergy to palonosetron and ondensetron
2.Use of antiemetics within 48 hours prior to surgery
3.Patient refusal
4.Patient with prolonged QT syndrome
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the efficacy of ondansetron versus palonosetron in preventing postoperative nausea and vomiting in the first 24 hours using three scoring systems (nausea score, postoperative vomiting score, and postoperative nausea and vomiting score) in patients undergoing elective otorhinolaryngology surgeries under general anaesthesiaTimepoint: at base line , 2 hours , 6 hours , 12 hours , 24 hours
- Secondary Outcome Measures
Name Time Method To measure the severity of nausea, need for rescue medication, patient’s satisfaction and incidence of adverse effects. <br/ ><br> <br/ ><br>Timepoint: 0 to 2 hrs, 2 to 6 hrs, 6 to 24 hrs