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To ensure informed voluntary participation, the study participants received an oral explanation of the objectives and procedures of the study.
All study participants gave written informed consent before participation; the study was approved by the Institutional Review Boards of the National Public Health Institute in Finland and the US National Cancer Institute.
Prior to their participation, the study risks, benefits and examination procedures were described to them.
Despite poor patient participation, the study reports that the trial outcomes are consistent with the results from the conventional trial.
Severe psychiatric or cognitive disorder, which in the opinion of the investigator would compromise participation the study.
When a patient is eligible for participation the study will be explained to them and Informed Consent will be asked.
Similar(50)
Participants' participation in the study was voluntary.
No eligible participant declined participation in the study.
All participants gave informed consent before participation in the study.
All participants had knowledge of their participation in the study.
Participants provided written consent for participation in the study.
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