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The threshold of inclusion is informed by expertise and instinct rather than being articulated a priori.
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Patients who were alive at the time of inclusion were informed about the study by a letter and given the option to withdraw.
Patients who met the inclusion criteria were informed with verbal and written information regarding the study and then both patients and their guardians were asked to give a written informed consent if they agreed to participate in this study.
Before inclusion, participants were informed of the study procedures and risks, signed a statement of informed consent and were approved for participation by a U.S. EPA physician.
Patients who met the inclusion criteria were informed about the study and were invited to participate.
Before inclusion, patients were informed that the trial compared two potentially beneficial interventions.
Participants meeting the inclusion criteria were informed about the study objectives and protocol.
Patients who met the inclusion criteria were informed about the study after which a signed consent was obtained.
Inclusion criteria were informed parental consent, neonates born at ≤ 34 weeks gestation, and birth weight ≤ 1500 g.
If there is a free bed in the orthogeriatric unit patients fulfilling the inclusion criteria are informed about the study and asked to participate.
A standardised procedure was developed to ensure that all the employees who met the inclusion criteria were informed, included and randomised.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com