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Evaluation of the administration of CoQ10 tablets in poisoning with aluminum phosphide tablets

Phase 3
Recruiting
Conditions
Poisoning with aluminum phosphide tablets.
Toxic effect of pesticides
Registration Number
IRCT20130917014693N14
Lead Sponsor
Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
50
Inclusion Criteria

People over 18 years old
People diagnosed with aluminum phosphide poisoning within 24 hours of being diagnosed with poisoning.
Signing the informed consent form by the patient or his / her legal guardian

Exclusion Criteria

Heart failure
Acute renal failure
Chronic liver failure
Chronic renal failure
History of acute myocardial infarction
Patients with a history of allergy to administered medicines

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Death rate. Timepoint: Duraing the study. Method of measurement: Using the patient's clinical record.
Secondary Outcome Measures
NameTimeMethod
Changes in the results of arterial blood gas analysis. Timepoint: On a daily basis from the beginning of the drug administration to the end of the study. Method of measurement: The GEM Premier 3000 device is used to measure arterial blood gases.;Duration of hospitalization. Timepoint: On a daily basis from the beginning of the drug administration to the end of the study. Method of measurement: Using the patient's clinical record.;Blood pressure. Timepoint: On a daily basis from the beginning of the drug administration to the end of the study. Method of measurement: Sphygmomanometer.
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