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The assessment of patient-reported outcomes (PROs) in clinical trials poses a number of potential problems. What happens when a patient reports a severe symptom and no one is monitoring that information; for example, when questionnaires are not reviewed until the end of a study? Do hospitals or researchers face liability if a patient reports suicidal thoughts on a questionnaire? http://jama.jamanetwork.com/article.aspx?articleid=1741830

Type

Journal

JAMA

Publisher

JAMA

Publication Date

25/09/2013

Volume

Vol 310, No12

Addresses

Derek Kyte: d.g.kyte@bham.ac.uk