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e-Prone Clinical Protocol

e-Prone Clinical Protocol

On this platform you will find information and resources that will enable you to learn about and implement the protocol of the study "Effect of Continuous Prolonged Prone Position versus Intermittent Daily Prone Position on Mortality in ARDS Patients: A Multicenter Randomized Controlled Trial."

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Responsible mpamthau@uc.cl
Last Update 04/29/2025
Completion Time 20 minutes
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e-Prone Clinical Protocol

Modelo sugerido para solicitud de consentimiento informado

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Recomendaciones para solicitud de consentimiento informado
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e-Prone Clinical Protocol
Modelo sugerido para solicitud de consentimiento informado

Download the PDF version


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e-Prone Clinical Protocol
Invitación a participar del estudio clínico - Caso familiar demandante de información
The following presents an example of how to carry out the authorization request procedure with the patient's designated family member when additional information is requested or further concerns are raised. English subtitles are available and can be activated in the video.
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e-Prone Clinical Protocol
Invitación a participar del estudio clínico - Caso estándar
Below is a standard example of how to carry out the procedure for requesting authorization from the patient’s legal representative. The video includes Spanish subtitles that can be activated.
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