Trials / Completed
CompletedNCT01440673
Aprepitant for Postoperative Nausea and Vomiting in Laparoscopic Hysterectomy
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 150 (actual)
- Sponsor
- Gachon University Gil Medical Center · Academic / Other
- Sex
- Female
- Age
- 21 Years – 60 Years
- Healthy volunteers
- Not accepted
Summary
* Gynecological surgery is associated with a high incidence of postoperative nausea and vomiting. * NK1 receptor antagonists such as aprepitant appear to be highly effective for treating acute and delayed emesis, and yet understanding of the efficacy of different doses of aprepitant is limited. * We performed a prospective, randomized, double-blinded placebo-controlled study of 123 female adults scheduled for laparoscopic hysterectomy who received 80 mg aprepitant, 125 mg aprepitant, or a placebo.
Detailed description
123 female patients (ages 21-60) undergoing laparoscopic hysterectomy 1. 80mg aprepitant 2. 125mg aprepitant 3. placebo Incidences of nausea, vomiting/retching, and use of rescue antiemetics were recorded at 0, 1, 2, 24, and 48 h after surgery.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Aprepitant | Aprepitant 80 mg, Aprepitant 125 mg |
Timeline
- Start date
- 2010-03-01
- Primary completion
- 2010-09-01
- Completion
- 2010-09-01
- First posted
- 2011-09-26
- Last updated
- 2011-09-26
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT01440673. Inclusion in this directory is not an endorsement.