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The effect of oral Aprepitant and Ondansetron injection on postoperative nausea and vomiting

Not Applicable
Conditions
nausea and vomitting.
Nausea and vomiting
Registration Number
IRCT2016120831302N1
Lead Sponsor
Vice President of Research, Kurdistan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
90
Inclusion Criteria

women between 18 to 50 years old with ASA class 1 and 2 with at least 2 criteria of APFEL (female; nonsmoker; motion sickness or PONV history; using opioids 100mcg fentanyl or equivalent )
Exclusion criteria: women under 18 or greater than 50 years old; AA class 3 or more; cholecystectomy in other anesthesia; systemic disease like diabetes; asthma; cardiovascular; reflux, severe obesity; pregnancy; breast feeding; hepatic and renal disease; neuromuscular disease; psychotic disease; addiction; acute cholecystitis.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ausea and vomitting. Timepoint: 6 and 24 hours after operation. Method of measurement: VAS criteria.
Secondary Outcome Measures
NameTimeMethod
Hospitalization period. Timepoint: at discharge time. Method of measurement: hospitalization days.
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