Selected article for: "block randomisation and eCRF provider study statistician access"

Author: Bird, Grace; Braithwaite, Irene; Harper, James; McKinstry, Steven; Koorevaar, Iris; Fingleton, James; Semprini, Alex; Dilcher, Meik; Jennings, Lance; Weatherall, Mark; Beasley, Richard
Title: Protocol for a randomised, single-blind, two-arm, parallel-group controlled trial of the efficacy of rhinothermy delivered by nasal high flow therapy in the treatment of the common cold
  • Document date: 2019_6_19
  • ID: x2xc1s14_161
    Snippet: A permuted block randomisation method stratified by duration of illness, lesser versus greater than or equal to one day, will be used to allocate participants to either treatment arm. The computergenerated sequence will be supplied by the study statistician, independent of the investigators. The eCRF system will conceal the allocations and will release a participant's randomisation outcome at the time of randomisation. The randomisation schedule .....
    Document: A permuted block randomisation method stratified by duration of illness, lesser versus greater than or equal to one day, will be used to allocate participants to either treatment arm. The computergenerated sequence will be supplied by the study statistician, independent of the investigators. The eCRF system will conceal the allocations and will release a participant's randomisation outcome at the time of randomisation. The randomisation schedule will only be accessed by the study statistician and the eCRF provider; study staff will not have access to the randomisation schedule.

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