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
| Type | Name | Description |
|---|---|---|
| DRUG | dexamethasone | dexamethasone 8 mg iv 2 minutes before induction of anesthesia |
| DRUG | Gabapentin | oral gabapentin 600 mg 1 hour before induction of anesthesia |
| DRUG | Aprepitant | oral 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.