Alternative consent methods used in the multinational, pragmatic, randomised clinical trial SafeBoosC-III
Abstract Background The process of obtaining prior informed consent for experimental treatment does not fit well into the clinical reality of acute and intensive care. The therapeutic window of interventions is often short, which may reduce the validity of the consent and the rate of enrolled partic...
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| Glavni autori: | , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BMC
2024-04-01
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| Serija: | Trials |
| Teme: | |
| Online pristup: | https://doi.org/10.1186/s13063-024-08074-0 |
| Oznake: |
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