Trials / Completed
CompletedNCT02040350
Is the WHO Recommended Dose of Pralidoxime Effective in the Treatment of Organophosphorus Poisoning?
Study Effect of WHO Recommended Dose of Pralidoxime in the Treatment of Organophosphorus Poisoning
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 100 (actual)
- Sponsor
- Sheri Kashmir Institute of Medical Sciences · Academic / Other
- Sex
- All
- Age
- 14 Years – 60 Years
- Healthy volunteers
- Not accepted
Summary
To evaluate the effectiveness of Pralidoxime, a drug used for treatment of pesticide poisoning (Organophosphorous poisonings)
Detailed description
The present study was designed to critically analyze the role of pralidoxime in patients with moderate to severe poisoning by dividing them into two comparable groups in all aspects and using WHO recommended dose of pralidoxime (30mg/kg bolus I.V over 20 min followed by 8mg/kg/hr continuous infusion). This dose and continuous infusion protocol is more likely to maintain adequate blood concentrations of pralidoxime throughout 24 hours and thus would avoid any failures in effectiveness of pralidoxime because of inconsistent blood levels.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Pralidoxime | Pralidoxime was compared to placebo to study the effects of the drug on mortatlity |
Timeline
- Start date
- 2012-04-01
- Primary completion
- 2013-08-01
- Completion
- 2013-11-01
- First posted
- 2014-01-20
- Last updated
- 2014-01-20
Locations
1 site across 1 country: India
Source: ClinicalTrials.gov record NCT02040350. Inclusion in this directory is not an endorsement.