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In both studies, trial benefits persisted further than expected beyond the intervention.
This trial benefits from rigorous design in terms of independent randomisation, blind rated assessments, and a clearly protocolised complex intervention.
The trial benefits from extensive DUP data from UK National EDEN sites in Cambridge, Cornwall, Blackburn, Blackpool, Burnley, Lancaster and Norwich [ 18].
The five most frequent topics were informed consent, early termination of a clinical trial, benefits and risks, human biological samples, and patient rights.
First, in comparison to earlier studies carried out on NET with children, this trial benefits from a comparatively large and inclusive sample drawn from immigrant children settled or seeking to settle in Finland.
In one trial, benefits of duration of mechanical ventilation were clinically relevant, with a mean reduction of 2.4 days [ 13] and up to 4 extra ventilator-free days in a subsequent trial [ 14].
Similar(51)
The trial benefited from a pragmatic setting, intention-to-treat analysis, blinding of outcome assessment and a broad socioeconomic spectrum of participants.
Designing and prioritizing successful clinical trials benefits from increased community physician input.
For operational research, the obligation to provide post-trial benefits is better articulated as an obligation to change treatment practice.
Post-trial benefits will not be provided through a state-run health care system after the VHX trial.
bThe 2013 Declaration of Helsinki gives the primary obligation for the provision of post-trial benefits to researchers, sponsors, and host country governments in Paragraph 34.
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