The efficacy of plasmapheresis in the treatment of patients poisoned with aluminum phosphide

Phase 2

Recruiting

• Conditions: Aluminum phosphide poisoning.; Toxic effect of pesticides

• Registration Number: IRCT20200507047344N2
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 5 January 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Aged between 20 and 65 years
Poisoned with aluminum phosphide
Patient/attendant consent to participate in the study

Exclusion Criteria

Any risk of coagulation disorders
History of chronic kidney failure

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Systolic blood pressure. Timepoint: Immediately upon arrival at the hospital and every hour to 6 hours after the intervention. Method of measurement: Sphygmomanometer.;?Diastolic blood pressure. Timepoint: Immediately upon arrival at the hospital and every hour to 6 hours after the intervention. Method of measurement: Sphygmomanometer.;Creatinine. Timepoint: Immediately upon arrival at the hospital and 12 hours after the intervention. Method of measurement: Blood test.;Sodium. Timepoint: Immediately upon arrival at the hospital and 12 hours after the intervention. Method of measurement: Blood test.;Magnesium. Timepoint: Immediately upon arrival at the hospital and 12 hours after the intervention. Method of measurement: Blood test.;Platelets. Timepoint: Immediately upon arrival at the hospital and 12 hours after the intervention. Method of measurement: Blood test.