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A literature review for trials using a fibreoptic intubation in a manikin and similar methodology demonstrated median intubation times ranging from 36 to 54 s.
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We searched MEDLINE, the Cochrane Library, all retrieved trials and pertinent reviews for trials published between 1981 and September 2002.
Approval for the study has been obtained from a National Health Service Research Ethics Committee with authority to review proposals for trials of a medical device in incapacitated adults.
Approval has been obtained from a National Health Service NHS Research Ethics Committeeee with authority to review proposals for trials of a medical device in incapacitated adults.
Patients will be informed of the strict confidentiality of their personal data collected for this trial, and that their medical records may be reviewed for trial purposes by authorized individuals.
Patients are informed about the strict confidentiality of their personal data within this trial, but their pseudonymised medical records may be reviewed for trial purposes by authorized individuals other than their treating physician.
The participants will be informed that their patient data will be held strictly confidential but that that their medical records may be reviewed for trial purposes by authorized individuals other than their treating physician.
They will be informed as to the strict confidentiality of their patient data, but that their medical records may be reviewed for trial purposes by authorised individuals other than their treating physician.
They will be informed about the strict confidentiality of their personal data, but that their medical records may be reviewed for trial purposes by authorised individuals other than their treating physician.
For example, while the United States Food and Drug Administration FDAA) has extensive regulations governing REC review for clinical trials conducted pursuant to an Investigational New Drug Application (IND), those regulations do not apply to foreign trials not conducted pursuant to an IND.
The percent agreement (HER2-positive vs. HER2-normal) between the original central review result and round-robin final HER2 result of the primary block (defined as the block used in the original central review for clinical trial eligibility; one per patient) was computed in the subsets of BCIRG-005 HER2-normal, N9831 HER2-normal, and N9831/BCIRG-006 HER2-positive specimens (all by central review).
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CEO of Professional Science Editing for Scientists @ prosciediting.com