Condition: Pelvic Tumor · Thoracic Tumor · Sponsor: University Medical Center Goettingen
This prospective registry-based trial will include patients with pelvic or thoracic tumors with an indication for radiotherapy treated with oART or IGRT. For the primary endpoint and the secondary clinical endpoints, the trial will compare oART versus IGRT, for technical endpoints the trial will compare the real oART scenario with two virtual (hypothetical) control scenarios. Primary endpoint: * 10% reduction in the rate of acute radiotherapy related toxicity (≥ CTCAE II°, v5.0) using oART Secondary endpoints: * Clinical endpoints: Tumor control, late toxicities compared to conventional irradiated patients, quality of life and patient-reported outcomes * Technical endpoints: Target volume, target coverage, dose to organs at risk, anatomical variability score
This description comes directly from the study's public registry record.
Laura Anna Fischer · +49 551 3964501 · laura-anna.fischer@med.uni-goettingen.de
Rami El Shafie · rami.elshafie@med.uni-goettingen.de
Always discuss trial participation with your own doctor first.
| University Medical Center, Departement of Radiation Oncology | Göttingen, Germany | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06185062