Health Condition 1: R688- Other general symptoms and signs
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: American society of Anesthesiologists (ASA) grade I and II Patients giving informed written valid consent. Either sex. Patients scheduled to undergo elective laparoscopic surgeries.
Exclusion criteria
Exclusion criteria: History of allergy to Ondansetron or Palonosetron. Patients posted for emergency surgery. Pregnant History of nausea and vomiting 24hrs prior to surgery. History of motion sickness.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the efficacy of ondansetron and palonosetron in reducing the incidence of postoperative nausea and vomiting.Timepoint: To compare the efficacy of ondansetron and palonosetron on the incidence of postoperative nausea and vomiting, the postoperative periods of 0-2 hours, 2-6 hours, and 6-24 hours should be considered. | — |
Secondary
| Measure | Time frame |
|---|---|
| To examine hemodynamic parameters & adverse effects in both groups.Timepoint: 0-2 hours, 2-6hours, 6-24hours postoperative period. | — |
Countries
India
Contacts
Gulbarga institute of medical sciences