Overview
Study to Know the Efficacy of Higher Doses of Pralidoxime in Patients of Organophpsphorus Poisoning.
Status:
Completed
Completed
Trial end date:
2003-06-01
2003-06-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to determine whether high doses of pralidoxime(PAM) are effective as compare to lower doses of PAM in the management of moderately sever organophosphorus poisoning patients.Phase:
N/AAccepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Giriraj HospitalTreatments:
Pralidoxime
Criteria
Inclusion Criteria:-patients with a history of poisoning by an organophosphorus pesticide and clinical
features of poisoning.
Exclusion Criteria:
patients who
- were under 12 years
- had chronic disease
- had malignancy
- were pregnant,
- presented more than 24 hrs post-ingestion,
- who could not be resuscitated successfully in the emergency room of our ospital