Clinical Trials Directory

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

TypeNameDescription
DRUGAprepitantAprepitant 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.

Aprepitant for Postoperative Nausea and Vomiting in Laparoscopic Hysterectomy (NCT01440673) · Clinical Trials Directory