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ISARIC/WHO Clinical Characterisation Protocol UK IRAS Ref. 126600/ 279826 SUMMARY INFORMATION SHEET & CONSENT FORM FOR ADULT PATIENTS DATA ONLY 30th August 2022. Version 10.2 Local lead investigator:
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Step 1: Start by obtaining the ISARICWHO Clinical Characterisation Protocol form.
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Step 3: Fill in your personal details accurately, including your name, contact information, and any other necessary identification details.
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Step 4: Provide information about your clinical presentation and symptoms. Be as detailed and specific as possible.
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Who needs isaricwho clinical characterisation protocol?

01
Healthcare professionals and researchers who are involved in clinical characterisation studies.
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Individuals who have been diagnosed with a particular illness or condition and are willing to contribute their data for research purposes.
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Public health organizations and institutes that are gathering data and conducting research on infectious diseases or other health-related issues.
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Regulatory bodies and government agencies that require comprehensive clinical data for monitoring and surveillance purposes.
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Medical practitioners and scientists interested in enhancing their understanding of certain diseases and their clinical characteristics.

What is ISARIC/WHO Clinical Characterisation Protocol (CCP) Form?

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The ISARIC-WHO Clinical Characterisation Protocol is a standardized research framework developed to enable the systematic collection of clinical data from patients suspected of having infectious diseases, particularly during outbreaks.
Researchers, clinicians, and healthcare institutions conducting studies or treating patients in the context of specific infectious disease outbreaks are required to file the ISARIC-WHO Clinical Characterisation Protocol.
To fill out the ISARIC-WHO Clinical Characterisation Protocol, investigators should follow the guidelines provided in the protocol manual, entering patient data systematically, ensuring comprehensiveness and accuracy.
The purpose of the ISARIC-WHO Clinical Characterisation Protocol is to facilitate the collection of detailed clinical information that can be used for better understanding disease progression, treatment outcomes, and public health responses during outbreaks.
Information that must be reported includes patient demographics, clinical history, symptoms, laboratory findings, treatments administered, and outcomes of the illness.
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