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The majority of the participants who were excluded from this study after the informed consent process either did not adhere to medication regimen or did not keep the scheduled appointment.
Any children whose parents did not actively provide their informed consent were excluded from the study.
Patients whose condition precluded the ability to give informed consent were excluded from the study.
Any service user who did not have capacity to provide informed consent was excluded from the study.
7 Patients with T4 tumors or without written informed consent were excluded from the sentinel lymph node protocol.
Subjects previously diagnosed with CRC and subjects unable to give informed consent were excluded from the study.
Patients with type 1 DM and those patients who could not provide informed consent were excluded from the study.
All patients who were on anti TB drugs and those who could not offer informed consent were excluded from the study.
People with mental illnesses that affected behavior, alcohol or drug abuse, or who refused to sign the informed consent were excluded from the study.
All non-pregnant women, pregnant women younger than 18 years or pregnant women who did not give written informed consent were excluded from this study.
Girls with visual impairment, evening class students and those who were critically ill and incapable to provide informed consent were excluded from the study.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com