Trials / Completed
CompletedNCT01543945
Prevention Post Operative Nausea Vomiting in Ambulatory Gynecologic Laparoscopy
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 340 (actual)
- Sponsor
- Prince of Songkla University · Academic / Other
- Sex
- Female
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare the incidence of Postoperative nausea and vomiting between the intervention group who received multimodal antiemetic management and the control group who did not get this protocol.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Dexamethasone | 4 mg iv before induction for high and extremely high risk |
| DRUG | Ondansetron | 4 mg iv before ended surgery 30 min |
| DRUG | Dimenhydrinate | 1 mg/kg iv before ended surgery 30 min |
Timeline
- Start date
- 2008-03-01
- Primary completion
- 2011-12-01
- First posted
- 2012-03-05
- Last updated
- 2012-07-31
Locations
1 site across 1 country: Thailand
Source: ClinicalTrials.gov record NCT01543945. Inclusion in this directory is not an endorsement.