Investigation of the effect of Trimetazidine in patients with Aluminum phosphide poisoning
- Conditions
- Patients with Aluminum phosphide poisoning.Poisoning by unspecified drugs, medicaments and biological substances, accidental (unintentional)T50.901
- Registration Number
- IRCT20211017052794N1
- Lead Sponsor
- Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 30
Consumption of oral form of Aluminium phosphide and referrs to Loghman Hospital under 24 hours and the presence of symptoms consistent with poisoning
Positive silver nitrate test
Carbon monoxide levels above 10 in non-smokers
Glomerular Filtration Rate(GFR) less than 30 (if available ),history of renal failure , history of liver failure , history of acute myocardial infarction, history of heart failure, history of congenital heart disease
Pregnancy and lactation
Refer to hospital after 24 hours
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Mortality. Timepoint: During hospitalization. Method of measurement: Death during admission.
- Secondary Outcome Measures
Name Time Method Admit duration. Timepoint: Period of time. Method of measurement: Daily chart.;Icu admission. Timepoint: Number of hospitalization days. Method of measurement: Daily chart.;Arrhythmia. Timepoint: Daily electrocardiogram/As long as the patient is being treated with trimetazidine. Method of measurement: Electrocardiogram.;Need for inotropic drugs. Timepoint: Number of hospitalization days. Method of measurement: Based on blood pressure less than 90 mmHg and inotrop drugs initiation recorded in the chart.;Left ventricle ejection fraction. Timepoint: Second day of admission. Method of measurement: Echocardiography.;Intubation. Timepoint: Hospital admission. Method of measurement: Number of intubation patients registered in the chart.