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Hemoperfusion for organophosphate poisoning in critically ill patients- A randomized trial.

Not Applicable
Recruiting
Conditions
Injury, Occupational Diseases, Poisoning
Registration Number
PACTR202009754904918
Lead Sponsor
Jalo
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria

All adult patients admitted to the ICU with a diagnosis of organophosphate poisoning will be included.
Age =18 years
Consistent History
Cholinergic toxidrome
Patient recruitment within 12 hours of ICU admission
Written informed consent

Exclusion Criteria

Patients with polypharmacy overdoses were excluded
Patients with a contra-indication to anticoagulation with heparin and enoxaparin

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ICU length of Stay
Secondary Outcome Measures
NameTimeMethod
Mortality ;Serum Organophosphate and Carbamate levels;Cost of ICU stay;Duration and Dose of antidote;Duration of Organ support;Motor Score;Complications
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