Clinical Trials Directory

Trials / Completed

CompletedNCT02597907

Postoperative Nausea and Vomiting: Ramosetron Plus Aprepitant vs Palonosetron Plus Aprepitant

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
88 (actual)
Sponsor
Kyungpook National University Hospital · Academic / Other
Sex
Female
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study was to compare the antiemetic efficacy of aprepitant plus palonosetron versus aprepitant plus ramosetron in high risk patients undergoing laparoscopic cholecystectomy.

Detailed description

The purpose of this study was to compare the antiemetic efficacy of aprepitant plus palonosetron versus aprepitant plus ramosetron in high risk patients undergoing laparoscopic cholecystectomy. Study is performed during 24 hours after surgery.

Conditions

Interventions

TypeNameDescription
DRUGaprepitantaprepitant 80 mg is given to all patients before surgery
DRUGpalonosetronpalonosetron 0.075 mg is given to patients in the aprepitant plus palonosetron group after induction of general anesthesia
DRUGRamosetronramosetron 0.3 mg is given to patients in the aprepitant plus ramosetron group after induction of general anesthesia

Timeline

Start date
2014-07-01
Primary completion
2015-05-01
Completion
2015-07-01
First posted
2015-11-05
Last updated
2017-04-25
Results posted
2017-04-25

Source: ClinicalTrials.gov record NCT02597907. Inclusion in this directory is not an endorsement.