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Randomized Trial of Acetylcysteine in Idiopathic Pulmonary Fibrosis

Randomized Trial of Acetylcysteine in Idiopathic Pulmonary Fibrosis

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_1530407058

Randomized Trial of Acetylcysteine in Idiopathic Pulmonary Fibrosis

About this item

Full title

Randomized Trial of Acetylcysteine in Idiopathic Pulmonary Fibrosis

Publisher

Waltham, MA: Massachusetts Medical Society

Journal title

The New England journal of medicine, 2014-05, Vol.370 (22), p.2093-2101

Language

English

Formats

Publication information

Publisher

Waltham, MA: Massachusetts Medical Society

More information

Scope and Contents

Contents

Acetylcysteine, which has been advocated as a treatment for patients with idiopathic pulmonary fibrosis, showed no benefit over placebo with respect to loss of lung function in such patients at 60 weeks.
Idiopathic pulmonary fibrosis is a chronic, progressive lung disease of unknown cause that is characterized by the histopathological or radiolo...

Alternative Titles

Full title

Randomized Trial of Acetylcysteine in Idiopathic Pulmonary Fibrosis

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_1530407058

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_1530407058

Other Identifiers

ISSN

0028-4793

E-ISSN

1533-4406

DOI

10.1056/NEJMoa1401739

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