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Patients with SUI will be randomized through a website according to a computer-generated randomization sequence.
After having properly checked all eligibility criteria, stratification parameters, and having obtained patient written consent, patients will be randomized through an electronic case-report form (eCRF), using a minimization technique.
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After informed consent is obtained participants are randomized through a computer-generated randomization sequence with stratification for centre, in one of the two groups.
Once women with discordant test results have given consent for the trial, they are randomized through a website, according to a computer-generated randomization sequence.
In the CC, the genetic background is randomized through the process of creating recombinant inbred lines (Churchill et al. 2004).
Patients were randomized through an interactive voice response system in a 1 1 ratio, using a permuted block algorithm.
Participants were randomized through the study database using a predefined order created by a biostatistician with the Clinical Translational Research Center CTRCClinical Translational Research Center CTRC
Individuals (n = 12,612) from North and South America, Europe, India, the Asia/Pacific region, and Australia were randomized through December 2005, with results to be reported in 2012.
If a participant has a definite osteophyte on any view in the symptomatic knee, the participant is randomized through the process described below.
Classrooms (n = 75) are randomized through an automated system to one of 3 study arms (200 children per arm): (1) POPS; (2) POPS + IYS; or (3) Usual HS Exposure.
After an initial assessment, all patients that fit the inclusion criteria will be randomized to two different groups through a computer-generated list unknown to the recruiters, as follows: Control group.
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