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About
Uni-centric, randomized, open-label, prospective interventional-comparative study, with a control arm (patients receiving standard preoperative information) and an experimental arm (patients receiving standard preoperative information and having access to a dematerialized educational video support).
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Inclusion criteria
for therapeutic purposes (in the case of proven tumor histology) or for diagnostic and therapeutic purposes (in the absence of proven histology, but strong suspicion, after validation by RCP),
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
226 participants in 2 patient groups
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Central trial contact
Mathilde Lefevre
Data sourced from clinicaltrials.gov
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