Comparison of Effect of ondansetron And Chlorpheniramine in controlling nausea in adults in emergency department
Phase 3
Recruiting
- Conditions
- ausea in emergency room patients.
- Registration Number
- IRCT20230726058930N4
- Lead Sponsor
- Ahvaz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 195
Inclusion Criteria
Satisfaction of patients to participate in the trial
to be at least 18 years old
The patient complains of nausea
Exclusion Criteria
trauma(specially abdomen)
continuous vomiting which persists 1 hour after admission
alcohol consumption
unstable hemodynamic
history of allergy to ondansetron or Chlorpheniramine
pregnancy
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The degree of change in the patient's nausea based on a scale from 1 to 10 in zero, 20 and 60 minutes. Timepoint: At the time of injection, 20 minutes and 60 minutes after. Method of measurement: Based on the visual analog scale questionnaire.
- Secondary Outcome Measures
Name Time Method