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Earlier Endpoints Are Required for Hemorrhagic Shock Trials among Severely Injured Patients
BACKGROUND: Choosing the appropriate endpoint for a trauma hemorrhage control trial can determine the likelihood of its success. Recent Phase 3 trials and observational studies have used 24-hour and/or 30-day all-cause mortality as the primary endpoint and some have not used exception from informed...
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| Publicado no: | Shock |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5392160/ https://ncbi.nlm.nih.gov/pubmed/28207628 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/SHK.0000000000000788 |
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