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N/A N=88 Randomized Quadruple-blind Prevention

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

Postoperative Nausea and Vomiting

Enrolled (actual)
88
Serious AEs
0.0%
Results posted
Apr 2017
Primary outcome: Primary: The Incidence of Postoperative Nausea and Vomiting — 5; 18 Participants — p=<0.05

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
aprepitant (Drug); palonosetron (Drug); Ramosetron (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
Female
Sponsor
Kyungpook National University Hospital
Primary completion
May 2015

Outcome Measures

OutcomeResultp-value
PRIMARY
The Incidence of Postoperative Nausea and Vomiting
5; 18 <0.05 sig

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.

Eligibility Criteria

Inclusion Criteria

  • Non smoking, female patients, scheduled for laparoscopic cholecystectomy

Exclusion Criteria

  • Patients with gastrointestinal disorder,
  • Patients with allergies to any study medication,
  • Patients who had received any sedatives, opioid, steroid or antiemetics within 24 h before surgery
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02597907). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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