Comparison of antivenin and placebo effectiveness in scorpion biting
Not Applicable
- Conditions
- Scorpion bite.Venom of scorpion
- Registration Number
- IRCT138812142337N2
- Lead Sponsor
- Vice-chancellor for Research, Iran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 432
Inclusion Criteria
scorpion biting
Exclusion criteria: critically ill patients (shock, life threatening manifestations of scorpion biting)
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Anaphylaxy. Timepoint: every 10 minute. Method of measurement: vital signs.;Improvement of symptoms. Timepoint: every 4 hours. Method of measurement: clinical presentation.;Adverse effects. Timepoint: every 4 hours. Method of measurement: blood and urine samples.
- Secondary Outcome Measures
Name Time Method Serum sickness. Timepoint: During 1 week after injection of antivenom. Method of measurement: Physical examination and Fever.