Condition: Oropharynx Cancer · Radiotherapy; Complications · Radiotherapy Side Effect · Sponsor: Centre hospitalier de l'Université de Montréal (CHUM)
This is a phase II randomized trial, where patients with histologically proven squamous cell carcinoma of oropharynx that have primary tumor (T3 - T4) in place, treated with curative intent chemoradiation, will be randomized to systematic mid-treatment MRI-based radiotherapy adaptation vs. standard of care. The primary objective is to compare patient-rated dysphagia (as assessed by the MD Anderson Dysphagia Inventory composite score at 6 months post-treatment in patients undergoing routine mid-treatment MR-guided radiotherapy adaptation vs. in patients receiving the current standard of care.
This description comes directly from the study's public registry record.
Contact details are listed per location below or on the registry record.
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| Austin Health | Melbourne, Australia | Not Yet Recruiting |
| Centre Hospitalier de l'Université de Montréal | Montreal, Quebec, Canada | Recruiting |
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Source record: clinicaltrials.gov/study/NCT04901234