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Effect of oral betahistin in reducing of nausea and vomiting after surgery

Phase 3
Conditions
Postoperative nausea and vomiting.
Nausea and vomiting
Registration Number
IRCT20201225049829N1
Lead Sponsor
Mazandaran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
120
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
Pregnancy
Patients with BMI> 35
High blood pressure, cardiovascular disease, diarrhea with respiratory problems
If the laparoscopic surgery becomes an open cholecystectomy

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severe nausea. Timepoint: At times 1, 3, 6, 12, 24, 48 after surgery. Method of measurement: NRS (numerical rating scale).;Vomiting. Timepoint: At times 1, 3, 6, 12, 24, 48 after surgery. Method of measurement: NRS (numerical rating scale).
Secondary Outcome Measures
NameTimeMethod
The amount of ondansetron and narcotics consumed. Timepoint: At times 1, 3, 6, 12, 24 and 48 hours after surgery. Method of measurement: Questionnaire.;Dry mouth. Timepoint: At times 1, 3, 6, 12, 24 and 48 hours after surgery. Method of measurement: Questionnaire.;Headache. Timepoint: At times 1, 3, 6, 12, 24 and 48 hours after surgery. Method of measurement: Questionnaire.;Itching. Timepoint: At times 1, 3, 6, 12, 24 and 48 hours after surgery. Method of measurement: Questionnaire.
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