Study to find out the safety and efficacy of Pralidoxime in the management of patients with acute organophosphorous pesticide poisoning
Phase 4
- Conditions
- Health Condition 1: null- Acute organophosphorous poisoning
- Registration Number
- CTRI/2014/02/004392
- Lead Sponsor
- JIPMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 150
Inclusion Criteria
1.Patients with organophosphate poisoning
2.Age > 18yrs
3.Presenting within 12 Hours of ingestion
Exclusion Criteria
1.Patients with mixed compound poisioning
2.Patients with carbamate poisioning
3.Intubated and mechanically ventilated before presentation
4.Received more than 1 dose of pralidoxime before randomization
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method