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Participant Information and Consent Form SUPR3D: A RANDOMIZED PHASE III TRIAL COMPARING SIMPLE UNPLANNED PALLIATIVE RADIOTHERAPY VERSUS 3D CONFORMAL RADIOTHERAPY FOR PATIENTS WITH BONE METASTASESPrincipal
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What is doajorgarticle18286917c39e446187c2652dd245661esupr-3d a randomized phase?
This is a phase of a clinical trial where participants are randomly assigned to different treatment groups.
Who is required to file doajorgarticle18286917c39e446187c2652dd245661esupr-3d a randomized phase?
The principal investigator or sponsor of the clinical trial is required to file the randomized phase.
How to fill out doajorgarticle18286917c39e446187c2652dd245661esupr-3d a randomized phase?
The randomized phase must be filled out according to the specific guidelines provided by the regulatory authorities.
What is the purpose of doajorgarticle18286917c39e446187c2652dd245661esupr-3d a randomized phase?
The purpose of the randomized phase is to evaluate the efficacy and safety of a new treatment compared to standard treatments or a placebo.
What information must be reported on doajorgarticle18286917c39e446187c2652dd245661esupr-3d a randomized phase?
The randomized phase must include information on the study design, treatment groups, patient demographics, endpoints, results, and adverse events.
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