Why transition from alternation to randomisation in clinical trials was madeBMJ 1999; 319 doi: https://doi.org/10.1136/bmj.319.7221.1372 (Published 20 November 1999) Cite this as: BMJ 1999;319:1372
- Iain Chalmers, director ([email protected])
- Cochrane Centre, Oxford OX2 7LG
EDITOR—It is time to put the record straight about ways of controlling selection bias when generating comparison groups in clinical trials. D'Arcy Hart has done history a great service by noting that Bradford Hill's motivation for replacing alternation with randomisation was “to better conceal the allocation schedule.”1 This is what Guy Scadding (who, with D'Arcy Hart, is the other surviving member of the team who designed the streptomycin trial) told Mike Clarke and me when we visited him on 10 June 1999, and what Bradford Hill told William Silverman and me when we visited him on 3 April 1982.
Bradford Hill's motivation for concentrating on the concealment of …
Log in using your username and password
Log in through your institution
Register for a free trial to thebmj.com to receive unlimited access to all content on thebmj.com for 14 days.
Sign up for a free trial