Pelvic Cancer Registry for Online Adapted Radiotherapy
Condition(s) studied
Study summary
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
Eligibility
Primary outcome measure(s)
- Rate of acute radiotherapy related toxicity — until 12 weeks post RT
10% reduction in the rate of acute radiotherapy related toxicity (≥ CTCAE II°, v5.0) using oART
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| University Medical Center, Departement of Radiation Oncology | Göttingen | Germany | Recruiting |
More University Medical Center Goettingen trials in Germany
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06185062 on ClinicalTrials.gov ↗ ← All trials in Germany