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A Phase III multigenre randomized clinical trial of RCHOP14 vs RCHOP21 in newly diagnosed diffuse large Cell lymphoma Patient initialsDate of birthCentreConsultantSex(dd/mm/YYY)1M, 2FTo randomize
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Registration and randomisation forms document is a formal record used in research studies to track participant registration and allocation to treatment groups.
Researchers and institutions conducting clinical trials or studies involving human participants are required to file this documentation.
To fill out the form, researchers must provide detailed information about the study, including participant criteria, randomisation methods, and consent processes.
The purpose is to ensure transparency, accountability, and proper tracking of participants in clinical trials for reliability and validity of results.
Information required includes study title, objectives, methods of randomisation, inclusion/exclusion criteria, and participant demographics.
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