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The genotypes from this study will be provided upon request to the authors.
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All custom scripts, codes and macros used for this study will be provided upon request from the corresponding author.
Through a donation in-kind from Common Sense Advisory, a report with the full results of the study will be provided free of charge to the public.
All adults participating in the study will be provided with a plain language statement and will provide informed written consent.
Summaries of the results from included studies will be provided and a list of all items reported by included studies will be compiled.
Feedback of key messages from the sub-study will be provided to participants at the end of the study, based on aggregated data.
Reasons for excluding potentially eligible studies will be provided.
The information obtained from 1st study group will be provided to the Competent Authority (Paul-Ehrlich-Institute) for a review.
From our knowledge, this study will be one of the most comprehensive studies in this population, and will provide an initial database along with the impetus to promote a multisite study.
Materials Study medications will be provided under the Australian Therapeutic Goods Administration Clinical Trials Notification scheme.
Study medication will be provided by the first author (SPK).
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CEO of Professional Science Editing for Scientists @ prosciediting.com