SalbutamolOP: Adding Nebulized Salbutamol to Intravenous Atropine and Oxygen in OP Poisoning

Sponsor
Sylhet M.A.G.Osmani Medical College (Other)
Overall Status
Completed
CT.gov ID
NCT02160548
Collaborator
University of Edinburgh (Other)
75
1
3
8
9.4

Study Details

Study Description

Brief Summary

We hypothesize that salbutamol will speed removal of alveolar fluid compared to atropine alone in OP poisoned patients. We propose to compare the effect of two stat doses of nebulized salbutamol (2.5 mg; 5.0 mg), with nebulized saline placebo, in symptomatic patients receiving standard resuscitation with atropine, oxygen, and fluids after poisoning with OP pesticides. 25 patients will be randomised to each arm (total 75 patients). Primary outcome will be oxygen saturation's over the following 60 min during resuscitation. Secondary outcomes will include atropine dose administered, speed to stabilization, aspiration or pneumonia, intubation, tachydysrhythmias, and mortality. A positive outcome will result in design of a large definitive phase III study.

Condition or Disease Intervention/Treatment Phase
  • Drug: Standard care
  • Drug: Standard care+ 2.5 mg Salbutamol
  • Drug: Standard care+ 5 mg Salbutamol
Phase 3

Detailed Description

Pesticide self-poisoning kills over 300,000 people every year (1). Most deaths occur in rural Asia where widespread use of pesticides to boost food production allows easy access at stressful times. The WHO now recognizes pesticide poisoning to be the single most important global means of suicide (2) Amongst pesticides, organophosphorus (OP) and carbamate insecticides are of most concern, causing about 2/3 of deaths (1,3). These insecticides inhibit the enzyme acetylcholinesterase (AChE), producing an 'acute cholinergic crisis' with reduced consciousness, bradycardia, hypotension, and acute respiratory failure. On arrival at hospital, patients are resuscitated with atropine and, for OPs, an oxime AChE reactivator (4). Unfortunately, this treatment is often inadequate and many still die (5). A recent Bangladeshi RCT showed that rapid resuscitation of patients with atropine saves lives (6). This study compared a faster 'doubling dose' method of atropinisation with a standard bolus method during resuscitation. It reported quicker stabilisation and a 14% absolute reduction in mortality.

Rationale: Atropine only stops production of fluid and does not speed its removal from the lung. Therefore a treatment that increases removal, to complement atropine-induced cessation of production, could reduce fluid in the lungs and speed return effective oxygen exchange. A single nebulised dose of the beta-adrenergic agonist salbutamol may increase removal since it increases alveolar fluid removal via the epithelial sodium channel. A pilot clinical study is required to test the hypothesis and to provide data for powering a large phase III RCT.

Research question: Will addition of the beta-adrenergic agonist salbutamol to atropine during resuscitation improve oxygenation, reduce the need for atropine, and speed stabilisation?

Objectives:General Objectives: To test the efficacy of salbutamol at increasing oxygenation and speeding resuscitation.

Specific Objectives: To test whether salbutamol alters dose of atropine administered and incidence of tachydysrhythmias.

Total duration of the study will be one year and all patients aged 12 years or older with clinical features of OP/carbamate poisoning requiring oxygen and atropine will be enrolled. The study will be done in three arms.

Study Design

Study Type:
Interventional
Actual Enrollment :
75 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effect of Adding Nebulized Salbutamol to Intravenous Atropine and Oxygen During Resuscitation of OP Pesticide Poisoned Patients
Study Start Date :
Apr 1, 2015
Actual Primary Completion Date :
Dec 1, 2015
Actual Study Completion Date :
Dec 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: 'Standard care'

Standard care= Intravenous fluids, Oxygen by face mask, Intubation if necessary, Mechanical ventilation (Engstrom Pro by GE) if necessary, Cardiac monitor (Infunix IP4050), Atropine (anti-muscarinic drug; G-Atropine) by intravenous route, Pralidoxime (acetylcholinesterase reactivating oxime drug; PAM-A) by intravenous route.

Drug: Standard care
Standard management for OP poisoning
Other Names:
  • Intravenous fluids
  • Intubation if necessary,
  • Mechanical ventilation if necessary (Engstrom Pro)
  • Atropine (anti-muscarinic; G-Atropine)
  • Pralidoxime (acetylcholinesterase reactivating oxime; PAM-A)
  • Oxygen by face mask by intravenous route,
  • Experimental: 'Standard care+ 2.5 mg Salbutamol'

    Standard care+ 2.5 mg Salbutamol= Nebulized salbutamol (Ventolin respiratory solution) 2.5 mg stat and once only with standard care

    Drug: Standard care+ 2.5 mg Salbutamol
    Ventolin respiratory solution 2.5 mg
    Other Names:
  • Ventolin
  • Experimental: 'Standard care+ 5 mg Salbutamol'

    Standard care+ 5 mg Salbutamol= Nebulized salbutamol (Ventolin respiratory solution) 5 mg stat and once only with standard care

    Drug: Standard care+ 5 mg Salbutamol
    Ventolin respiratory solution 5 mg
    Other Names:
  • Ventolin
  • Outcome Measures

    Primary Outcome Measures

    1. Improvement of oxygen saturation [60 minutes]

      Improvement of oxygen saturation from the base line to normal level after adding nebulized salbutamol to regular I/V atropine and oxygen therapy.

    Secondary Outcome Measures

    1. Heart rate, respiratory rate and Blood pressure [60 minutes]

      Settlement of heart rate, respiratory rate and blood pressure to normal range after adding salbutamol to regular management.

    Other Outcome Measures

    1. Atropine dose [120 minutes]

      Requirement of total atropine dose until full atropinization (before put in to maintenance dose) after adding nebulized salbutamol

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    12 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • age 12 yrs or older

    • clinical features of OP poisoning

    • requiring oxygen and atropine and give consent

    Exclusion Criteria:
    • age 11 yrs or younger

    • no requirement for atropine

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Sylhet M.A.G.Osmani Medical College Hospital Sylhet Bangladesh 3100

    Sponsors and Collaborators

    • Sylhet M.A.G.Osmani Medical College
    • University of Edinburgh

    Investigators

    • Principal Investigator: Fazle R Chowdhury, FCPS, Consultant, Medicine, Sylhet M.A.G.Osmani Medical Collge, Sylhet, Bangladesh
    • Principal Investigator: Michael Eddleston, PhD, Professor of Clinical Toxicology, University of Edinburgh

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Dr. Fazle Rabbi Chowdhury, Consultant, Medicine, Sylhet M.A.G.Osmani Medical College
    ClinicalTrials.gov Identifier:
    NCT02160548
    Other Study ID Numbers:
    • Medicine SOMCH
    First Posted:
    Jun 10, 2014
    Last Update Posted:
    Dec 29, 2015
    Last Verified:
    Dec 1, 2015
    Keywords provided by Dr. Fazle Rabbi Chowdhury, Consultant, Medicine, Sylhet M.A.G.Osmani Medical College
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 29, 2015