Comparison of the therapeutic effect of injectable pantoprazole and famotidine in patients with epigastric pai
Phase 3
Recruiting
- Conditions
- epigastric pain.Pain localized to upper abdomenR10.1
- Registration Number
- IRCT20230614058478N1
- Lead Sponsor
- Zahedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Patients with epigastric pain referred to the emergency department of Khatam Zahedan Hospital in 1401
Exclusion Criteria
- Unwillingness to participate in the study
Pregnancy, patients with unstable vital signs, receiving antacids
Receiving antacid/H2 receptor blockers/PPI within two hours before ED visit, known allergy to study agents
Epigastric pain suspected of MI
Age over 60 and under 18, cholecystitis, suspected dissection
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain intensity after drug injection. Timepoint: 0-30-60 Minutes after receiving the medicine. Method of measurement: Assessing pain based on what is visible on the patient's face (VAS).
- Secondary Outcome Measures
Name Time Method