Study of effectiveness of propofol dosage in prevention of nausa and vomiting in some surgeris
Phase 3
- Conditions
- Condition 1: Nausea. Condition 2: Vomit.
- Registration Number
- IRCT20160307026950N21
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 48
Inclusion Criteria
The person should not have received any sedative or narcotic drugs
No gastrointestinal problems such as reflux
Patients should be between 18 and 65 years old.
Having a informed consent to enter the research
Exclusion Criteria
If there is any change in the relaxation method and the change in the surgical method, the patient should be excluded from the study.
The patient's age is more than 65 years
The patient's age is less than 18 years
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ausea score based on VAS criteria. Timepoint: During recovery time after surgery. Method of measurement: questionnaire.;To vomit or not to vomit. Timepoint: During recovery time after surgery. Method of measurement: questionnaire.
- Secondary Outcome Measures
Name Time Method