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IS ARIC/WHO Clinical Characterization Protocol UK IRAS Ref. 126600/ 279826 INFORMATION SHEET & CONSENT FORM FOR EXISTING DATA FOR ADULT PATIENTS DISCHARGED HOME 30th August 2022. Version 10.2 Local
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The isrctn66726260 clinical characterisation protocol outlines the details of a clinical study, including the objectives, methodology, and statistical analysis plan.
Researchers conducting the clinical study are required to file the isrctn66726260 clinical characterisation protocol.
The isrctn66726260 clinical characterisation protocol should be filled out according to the specific guidelines provided by the regulatory authorities or the institution overseeing the study.
The purpose of isrctn66726260 clinical characterisation protocol is to clearly define the parameters of the study and ensure that it is conducted in a rigorous and ethical manner.
The isrctn66726260 clinical characterisation protocol must include details such as study objectives, study population, intervention, outcome measures, and statistical analysis plan.
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