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According to the Cochrane risk of bias tool, the two common biases (unclear risk of bias) were selection bias (lack of specification of allocation concealment) and detection bias (lack of specification about blinding of outcome assessment; figure 2 and supplementary table 1).
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"[T]he bill's specification of budget allocations to each NSF directorate would significantly impede NSF's flexibility to deploy its funds to support the best ideas," according to the board's statement.
Although all included trials were randomized, double blinded and placebo controlled, specification of randomization and allocation concealment methods were different from each other.
These features include: true randomisation, concealed allocation, specification of eligibility criteria, blind outcome assessment, patient blinding, blind analysis and intention-to-treat analysis.
The RCT design includes key methodological features that have been recognized as important in minimizing bias in clinical trials: true randomization, concealed allocation, specification of eligibility criteria, blind outcome assessment, blind analysis and intention-to-treat analysis.
The RCT design includes key method features that have been recognised as important in minimising bias in clinical trials: true randomisation, concealed allocation, specification of eligibility criteria, blind outcome assessment, blind analysis and intention-to-treat analysis.
The trial includes key methodological features that have been recognised as minimising bias in clinical trials: true randomisation, concealed allocation, specification of eligibility criteria, blind outcome assessment, patient blinding, blind analysis and intention-to-treat analysis.
The RCT design includes key methodological features that have been recognized as important in minimizing bias in clinical trials: true randomization, concealed allocation, specification of eligibility criteria, and intention-to-treat analysis [ 41].
The trial includes key methodological features that have been recognised as minimising bias in clinical trials: true randomisation, concealed allocation, specification of eligibility criteria, blind outcome assessment, blind analysis and intention-to-treat analysis.
The organization includes functional specification, partition, allocation, and scheduling of pipeline.
The availability of this framework can facilitate the early identification and specification of the system portability NFR and their detailed allocation as specific portability functions to be handled by the specified allocation to hardware or software, or a specific combination of the two.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com