Comparison study of effect of ceftriaxone versus ciprofloxacin treatment on dysentery in childre
Phase 2
- Conditions
- Acute hemorrhagic gastroenteritis.Infectious gastroenteritis and colitis, unspecified
- Registration Number
- IRCT20231119060110N1
- Lead Sponsor
- Gorgan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 196
Inclusion Criteria
Not receiving antibiotics during the last week
Consent to participate in the study
Sensitivity to both ceftriaxone and ciprofloxacin in the initial antibiogram
Exclusion Criteria
Any sensitivity to fluoroquinolones and cephalosporins
Immune deficiency disease and malnutrition in children
No follow up and Low drug compliance of the patient in the 5-day period of treatment
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Acute bloody diarrhea frequency and severity. Timepoint: 3 days and 5 days after the start of treatment. Method of measurement: By asking the patient and parents.
- Secondary Outcome Measures
Name Time Method