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Trials|May 14, 2010
Assessing the potential for outcome reporting bias in a review: a tutorialKerry Dwan, Carrol Gamble, Ruwanthi Kolamunnage-Dona, et al.
Trials|April 18, 2014
Risk-proportionate clinical trial monitoring: an example approach from a non-commercial trials unitCatrin Tudur Smith, Paula Williamson, Ashley Jones, et al.
Pediatrics|October 7, 2015
Deferred Consent for Randomized Controlled Trials in Emergency Care SettingsKatie Harron, Kerry Woolfall, Kerry Dwan, et al.
HRB Open Research|May 6, 2022
A concept analysis of 'trial recruitment' using the hybrid modelHannah Delaney, Declan Devane, Andrew Hunter, et al.
Trials|January 27, 2015
The natural history of conducting and reporting clinical trials: interviews with trialistsRebecca M D Smyth, Ann Jacoby, Douglas G Altman, et al.
Clinical Trials (London, England)|November 14, 2023
Determining a risk-proportionate approach to the validation of statistical programming for clinical trialsCarrol Gamble, Steff Lewis, Deborah Stocken, et al.
Clinical Linguistics & Phonetics|May 7, 2020
Adding a fourth rater to three had little impact in pre-linguistic outcome classificationChristina Persson, Elizabeth J Conroy, Carrol Gamble, et al.
Plos One|August 8, 2012
Making co-enrolment feasible for randomised controlled trials in paediatric intensive careKatie Harron, Twin Lee, Tracy Ball, et al.
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