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All participants gave their free informed consent, after being thoroughly informed on the purpose, requirement, and procedures of the survey.
This assessment process selected six patients for the trial who agreed to take part as transplant recipients or as non-operated controls after being thoroughly informed of the trial and its attendant risks.
From December 2001 to November 2003, 36 patients with histologically proven gastric cancer, locally unrecsectable, recurrent after surgery or with metastatic localisations entered the study, after being thoroughly informed of the study design, benefits and risks according to the guidelines of local ethic committee and the Declaration of Helsinki Principles, and all of them signed their consent.
Moreover, oncology patients were found to be more than willing to participate in decision making after being thoroughly informed (van Tol-Geerdink et al, 2006).
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Patients were thoroughly informed about the procedures and written informed consent was obtained from each of them.
All of the informants spoke Swedish and were thoroughly informed about the aim of the study.
They were thoroughly informed about the study and signed an informed consent if they were willing to participate.
Before participation, each subject was thoroughly informed about the procedures and provided written informed consent prior to testing.
On the day of examination, the subjects were thoroughly informed of the study and they signed an informed consent form.
Before the start of the study, all participants were thoroughly informed about potential risks and thereafter signed an informed consent document.
All farmers were thoroughly informed about the project prior to the herd visit and gave their informed consent for the sampling of fecal specimens from their animals and for completion of a questionnaire regarding herd management practices.
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CEO of Professional Science Editing for Scientists @ prosciediting.com