IRCT20201225049829N1CompletedPhase 3
Effect of oral betahistin in reducing of nausea and vomiting after laparoscopic cholecystectomy with general anesthesia
Trial Snapshot
- Phase
- Phase 3
- Status
- Completed
- Enrollment
- 120
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 15 years to 60 years (—)
- Sex
- All
Inclusion Criteria
- •The patient's desire to participate in the study and gain informed consent
- •Candidate for elective laparoscopic cholecystectomy
- •Age between 15 to 60 years
- •No history of betahistine allergy
- •No history of gastrointestinal disease and cardiovascular disease and respiratory problems
Exclusion Criteria
- •Patients with uncontrolled diabetes
- •Underlying gastrointestinal disease
- •History of nausea and vomiting and taking anti-nausea and vomiting drugs in 24 hours before surgery
- •Middle ear disease
- •Patients with BMI> 35
- •High blood pressure, cardiovascular disease, diarrhea with respiratory problems
- •If the laparoscopic surgery becomes an open cholecystectomy
Investigators
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