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6 days ago · If only regarding consent as necessary to inform about added risks of experimentation, consent may be waived or simplified in pragmatic trials between low-risk ...
3 days ago · One of the key legal and ethical barriers to conducting the trials was the Norwegian Health Research Act, which demands informed consent from all participants ...
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6 days ago · Obtaining informed consent isn't going to be pragmatic; it is time-consuming, challenging, and individualized. Constrained funding in the feasibility phase ...
21 hours ago · Steps should be taken to ensure that patients who are unable to sign have a valid proxy method of giving their informed consent to be eligible to participate ...
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4 days ago · Pragmatic trial elements included using broad eligibility criteria, enrolling all Danish citizens fulfilling these criteria, not requiring informed consent or ...
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3 days ago · Patients choosing to participate will provide written informed consent and have the possibility to withdraw their participation at any time without the need to ...
7 days ago · With participant consent, we provided feedback to referring physicians by email about the successful enrollment of referred participants and data on ...
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6 days ago · All participants included in the study provided written informed consent. The study was approved by the Johns Hopkins Medicine institutional review board.
4 days ago · Pragmatic trials are designed to determine how well interventions work in clinical practice under everyday conditions. The multi-strategy intervention has two ...
Missing: Low always
6 days ago · We continue to suggest against treating patients who are not at high risk for severe disease.
Missing: always consent