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Since the patients in this study were incapable of granting informed consent, the investigators obtained this from the patients' legal guardians or by healthy proxy, before proceeding with the advised treatment.
After granting informed consent, all patients were instructed to store and use their eye drops at room temperature and to return all used medication bottles between day 28 and day 34 after opening.
As the patients in this study were incapable of granting informed consent, investigators therefore obtained informed consent from the subject's legal guardian or healthy proxy before accepting the advised treatment.
Because of the nature of patients' injuries, subjects in this clinical study were incapable of granting informed consent.
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All participants received a complete description of the study and granted informed consent.
All participants received a complete description of the study and granted informed consent, and the project was approved by the Ethics Committee of the "Sapienza" University of Rome, Polo Pontino.
Among these, 803 (63.0%) attended enrollment sessions, granted informed consent, and were enrolled.
After ethical committee approval had been granted, informed consent was obtained from 262 employees who started treatment.
All patients granted informed consent before participating in a comprehensive baseline evaluation of their clinical and psychosocial characteristics conducted by a physician and trained research assistants.
Aliquots of normal bone marrow were obtained from four normal allogenic bone marrow donors granting written informed consent and as approved by the Johns Hopkins Medical Institute Institutional Review Board (J0002).
All eligible patients granting signed informed consent were followed for 12 months.
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CEO of Professional Science Editing for Scientists @ prosciediting.com