SOPs and templates On this page, you will find standard operating procedures and templates for principal investigators and coordinators in the SafeBoosC-IIIv trial. Page ContentStandard operating proceduresAssessment of the primary outcomeBlinding of the primary outcome assessmentDelegation logDeletion of data due to withdrawal of consent or declined participationHypoxic thresholds for cerebral oximetersList of data needed for eCRF entryManual for data entries in OpenClinicaNIRS device and sensor handlingScreening and randomisationSubstudies and subsequent publicationsTasks for principal investigatorsTreatment guidelineTemplatesDelegation logParticipant inclusion listPrimary outcome logSite collaboration agreement Last updated: 17. February 2025 Responsible editor Webgruppen på Rigshospitalet Please give your consent in order to send your message. Please enter a valid email address. Note: This mail is not secure. Your email should therefore not include civil registration numbers or health information.Read how to send secure digital post:https://www.regionh.dk/securemail Write your message: Write your email (Must be filled out): If you wish to attach one or more files you will need to login first. Create account or log in I hereby give my consent to the Capital Region of Denmark to process the information in my enquiry for professional purposes only. Read the terms for your consent No e-mail has been registred for this user/group