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Study to Know the Efficacy of Higher Doses of Pralidoxime in Patients of Organophpsphorus Poisoning.

Primary Purpose

Acute Organophosphorus Pesticide Poisoning

Status
Completed
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Pralidoxime(drug)
Sponsored by
Giriraj Hospital
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Organophosphorus Pesticide Poisoning focused on measuring Organophosphorus poisoning, Atropine, Pralidoxime, Intermediate syndrome.

Eligibility Criteria

12 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Giriraj Hospital and Intensive Care Unit.

Outcomes

Primary Outcome Measures

Median atropine dose required in first 24 hours
proportion of patients who required intubation or developed intermediate syndrome
number of days ventilated and required ICU care

Secondary Outcome Measures

pneumonia (aspiration or ventilator-associated)
mean systolic and diastolic blood pressure (BP) in first 24 hours
case fatality

Full Information

First Posted
June 5, 2006
Last Updated
June 5, 2006
Sponsor
Giriraj Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00333944
Brief Title
Study to Know the Efficacy of Higher Doses of Pralidoxime in Patients of Organophpsphorus Poisoning.
Official Title
Effectiveness of High Dose Pralidoxime in the Treatment of Organophosphorus Pesticide Poisoning - a Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2000
Overall Recruitment Status
Completed
Study Start Date
May 2000 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
June 2003 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Giriraj Hospital

4. Oversight

5. Study Description

Brief 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.
Detailed Description
Standard treatment of organophosphorus pesticide poisoning involves administration of intravenous atropine and oximes to counter acetylcholinesterase inhibition.1 Treatment with atropine is well established, but the efficacy and dosage schedule of oximes are controversial.2-5 A dose of 1g every four to six hours has been the standard regimen in Asian district hospitals but many clinicians remain unconvinced by its effectiveness.3 Randomised controlled trials (RCT) performed in Vellore during the nineties compared a 12g infusion over 3-4 days with a 1g bolus dose and then with placebo.6,7 The authors reported no benefit from pralidoxime and an increased mortality in those receiving the infusion, and have stated that pralidoxime should not be given to organophosphorus poisoned patients.2 Others consider that the dosage regimen was not ideal, with therapeutic concentrations being obtained rarely during the treatment.3,4 Furthermore, many patients presented late and had taken dimethyl pesticides - a class that does not respond well to oximes after several hours - biasing the study against finding benefit. The proposed minimum effective plasma levels for pralidoxime of 4 mg/L were based on in vitro and animal experiments by Sundwall.8 Recent evidence, however, suggests that higher blood concentrations of pralidoxime are needed to antagonise the toxic effects of many pesticides and that a bolus loading infusion followed by a maintenance infusion would be the best regimen.9 The WHO have proposed that patients receive around 30mg/kg pralidoxime salt as a loading dose followed by an infusion of at least 8mg/kg/hr (roughly equivalent to 1-2 g bolus followed by 0·5 g/h in a 50kg south Asian patient).9,10 However, no trials have yet been performed to determine whether such a regimen reduces morbidity and mortality in severely poisoned patients.3 Since organophosphorus pesticides kill hundreds of thousands of people in rural Asia every year, it is essential to determine whether it benefits or harms such poisoned patients. Our hospital has typically used a regimen of 1g q4h in organophosphorus poisoned patients but we were unconvinced about the effectiveness of this expensive drug since many patients required ventilation for >10 days. We informally treated several patients with the WHO-recommended regimen but saw little benefit. Since pralidoxime has a high therapeutic index, we then decided to conduct a RCT with still higher doses, i.e. to compare a 1 g infusion every hour (q1h, 24 g/day) with 1g every four hours (q4h, 6 g/day), after a 2 g loading dose, to assess the effectiveness of high dose pralidoxime in organophosphorus poisoned patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Organophosphorus Pesticide Poisoning
Keywords
Organophosphorus poisoning, Atropine, Pralidoxime, Intermediate syndrome.

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Pralidoxime(drug)
Primary Outcome Measure Information:
Title
Median atropine dose required in first 24 hours
Title
proportion of patients who required intubation or developed intermediate syndrome
Title
number of days ventilated and required ICU care
Secondary Outcome Measure Information:
Title
pneumonia (aspiration or ventilator-associated)
Title
mean systolic and diastolic blood pressure (BP) in first 24 hours
Title
case fatality

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kirti S Pawar, MBBS,DA
Official's Role
Principal Investigator
Facility Information:
Facility Name
Giriraj Hospital and Intensive Care Unit.
City
Baramati. Pune District.
State/Province
Maharashtra.
ZIP/Postal Code
413 102.
Country
India

12. IPD Sharing Statement

Citations:
PubMed Identifier
17174705
Citation
Pawar KS, Bhoite RR, Pillay CP, Chavan SC, Malshikare DS, Garad SG. Continuous pralidoxime infusion versus repeated bolus injection to treat organophosphorus pesticide poisoning: a randomised controlled trial. Lancet. 2006 Dec 16;368(9553):2136-41. doi: 10.1016/S0140-6736(06)69862-0.
Results Reference
derived

Learn more about this trial

Study to Know the Efficacy of Higher Doses of Pralidoxime in Patients of Organophpsphorus Poisoning.

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