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Results: Eighteen patients, ten males, were purposefully selected for the primary study.
An affirmative response to any of these exclusionary conditions rendered a potential participant ineligible for the primary study.
In the following section we first describe the recruitment procedures for the primary study, then describe how the sub-sample was derived for the present study.
The protocol for the primary study and supporting CONSORT checklist are available as supporting information; see Checklist S1 and Protocol S1.
JGM was responsible for the primary study design and supervision of data collection.
For the primary study group, levels of serum CCL3 did not differ between the two groups.
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OCT was required for study entry and for determination of the primary study endpoint.
Please see reference [26] for a detailed description of the primary study and dataset.
Ethics approval was obtained for all of the primary studies (Table 1).
The second phase, Data Collection, comprises the execution of the Systematic Mapping, during which the search for the primary studies is performed and the inclusion/exclusion criteria are used in order to select relevant studies according to the research questions.
Section 4 presents the statistics for the primary studies, Section 5 answers various research questions, Section 6 discuss the external threats to validity, and, finally, Section 7 concludes the presentation.
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CEO of Professional Science Editing for Scientists @ prosciediting.com