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Many patients show relief from symptoms within 60 days when treated with other traditional anti-inflammatory agents such as NSAIDs, and the same would be expected of the study treatment.
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The adverse events in placebo groups mirrored the adverse events expected of the active medication studied, confirming that pretrial suggestions induce the adverse events in placebo-treated patients.
Although the results for the psychological variables were generally not as strong as had been expected, aspects of the study design may have resulted in an underestimate of their effects.
The expected duration of the study is 5 years.
The expected duration of the study depends on the results of the screening tests during pregnancy.
The TCPS requires that the expected duration of the study be presented and this was present in all consent forms.
According to the simulations assuming equivalent efficacy (or a "true" HR of 1), the expected power of the study to demonstrate noninferiority was only 69%.
Responses were durable, lasting a median 64 days, considering the advanced disease and limited expected survival of the study population.
The expected duration of the study for each patient was up to 16 days, which included a 14-day post-treatment safety follow-up.
Consequently, one of the expected applications of the study's results is to increase the number of validated tools available for future use in epidemiological and clinical studies in Spanish adolescents.
We will explain the study in detail and provide them with a full information package describing the aims, methods, and expected outcomes of the study.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com