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
| Type | Name | Description |
|---|---|---|
| DRUG | aprepitant | aprepitant 80 mg is given to all patients before surgery |
| DRUG | palonosetron | palonosetron 0.075 mg is given to patients in the aprepitant plus palonosetron group after induction of general anesthesia |
| DRUG | Ramosetron | ramosetron 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.