Clinical Trials Directory

Trials / Completed

CompletedNCT02525848

Aprepitant Versus Gabapentin Prophylaxis for Postoperative Nausea and Vomiting in Laparoscopic Gynecological Surgeries

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
150 (actual)
Sponsor
Assiut University · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

To evaluate the efficacy of pre-empetive administration of Aprepitant, Versus Gabapentin prophylaxis for reducing the incidence of postoperative nausea and vomiting in Laproscopic gynacological surgeries.

Detailed description

Postoperative nausea and vomiting (PONV) is frequently encountered in the surgical recovery room. Laparoscopic surgery is one important risk factor for increased incidence of PONV. Gabapentin, an anticonvulsant with known postoperative analgesic properties, has shown some activity against PONV. Results from clinical trials evaluating the anti-emetic efficacy of gabapentin are conflicting. Aprepitant, a neurokinin-1 (NK1) receptor antagonist, blockades the central effects of substance P. Substance P is a neurotransmitter found in central areas associated with emesis such as the dorsal vagal complex and area postrema.

Conditions

Interventions

TypeNameDescription
DRUGdexamethasonedexamethasone 8 mg iv 2 minutes before induction of anesthesia
DRUGGabapentinoral gabapentin 600 mg 1 hour before induction of anesthesia
DRUGAprepitantoral aprepitan 80mg 1 hour before induction of anesthesia.

Timeline

Start date
2015-08-01
Primary completion
2016-03-01
Completion
2016-03-01
First posted
2015-08-18
Last updated
2016-03-24

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT02525848. Inclusion in this directory is not an endorsement.