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In response to how informed consent is obtained, 34% of the respondents described it as follows; consent is got by the admitting nurse/doctor; by signing the consent form; obtained verbally; and implied consent.
Response rates were as follows: consent to contact patients was 92%, response to initial family history questionnaire was 65%, response to risk factor questionnaires was 73% of all eligible, and donation of a blood sample was 63% of all eligible.
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Following consent the interview questions were emailed in order to allow time to consider responses.
Following consent, they performed a brief navigation practice to increase familiarity with the navigation controls.
Following consent, all patients were attached to the EEDD and a "measurement" was made to determine the "location" of their ETTs.
Following consent, participants completed the main baseline questionnaire.
Following consent, interviews were audio-recorded and transcribed verbatim.
Following consent, participants completed psychological and physical evaluations.
Following consent a 2-hour hemoperfusion with LPS adsorber was began in five patients [ 2].
Following consent, the participant will be assessed for eligibility and potential enrollment in the trial.
Following consent, patients were randomised to intervention or no intervention (1 : 1) by contacting the CRUK Clinical Trials Unit (CTU).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com