The Australasian Clinical Toxicology Investigators Collaboration Randomized Trial of Different Loading Infusion Rates of N-Acetylcysteine
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Author contributions: FK, AD, IMW, NB, LM, AG, and BC conceived the study, designed the trial, and helped obtain ethics approval in their respective centers. FK, AD, IMW, NB, LM, AG, and BC supervised the conduct of the trial and data collection. BT, AD, and IMW provided statistical advice on study design and helped analyze the data; FK drafted the manuscript, and all authors contributed substantially to its revision. All authors take responsibility for the paper as a whole.Funding and support: The research study was not financially supported. After data collection, the statistical analysis was performed by CMAX, Institute of Drug Technology, Adelaide, South Australia and paid for by Cumberland Pharma, Nashville, TN.
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PII: S0196-0644(04)01326-5
doi:10.1016/j.annemergmed.2004.08.040
© 2005 American College of Emergency Physicians. Published by Elsevier Inc. All rights reserved.
