Expired Study
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Durham, North Carolina 27710


Purpose:

We hypothesize that the combination of aprepitant with dexamethasone will provide significantly improved prophylaxis against Postoperative nausea and vomiting compared with the combination of ondansetron and dexamethasone, in patients undergoing craniotomy under general anesthesia.


Criteria:

Inclusion Criteria: A patient is eligible for inclusion in this study if all of the following criteria apply: - Age: 18-75 years of age - Surgery: craniotomy under general anesthesia. - ASA Status: ASA: I, II, or III - Language: Fluent in the English language - Informed Consent: Written informed consent must be obtained. Exclusion Criteria: A patient will not be eligible for inclusion in this study if any one or more of the following criteria apply within thirty days of patient enrollment in this clinical trial: - Medical: Any condition that may impair a patient's ability to complete any of the study assessments or confound interpretation of results. - Hypersensitivity: Patient has a known immediate or delayed hypersensitivity reaction or known idiosyncrasy to any of the two study medications, ondansetron, or aprepitant. - Other Drugs: Patients should not be taking medications with known antiemetic properties (phenothiazines, butyrophenones, antihistamines), nor should they receive metoclopramide, or other antiemetics preoperatively or 12 hours before the scheduled surgical procedure. - Pregnant or lactating females: A pregnancy test will be performed within 24 hours of entering the study for females of childbearing potential. - Substance Abuse: Clinically significant abuse of substances (alcohol, illicit or prescribed medications) such that the patient is unable to provide informed consent or reliably complete any of the study assessments. - Psychiatric Disease: History of a psychiatric illness that may impair the patient's ability to provide informed consent or complete any of the study assessments. - Nausea verbal rating score (VRS): A VRS nausea score > 3 (scale 0-10) in the preoperative holding area before pretreatment with the study medications.


NCT ID:

NCT00734929


Primary Contact:

Principal Investigator
Ashraf S Habib, MBBCH, FRCA
Duke University


Backup Contact:

N/A


Location Contact:

Durham, North Carolina 27710
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: March 16, 2018

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