Ireland
--:--IST
Recruiting Observational

Pelvic Cancer Registry for Online Adapted Radiotherapy

NCT06185062 · tracked via the Priya Life Science Germany tracker
Phase
Observational
Started
2024-01-01
Last updated
2024-02-08

Condition(s) studied

Pelvic TumorThoracic Tumor

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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
INCLUSION CRITERIA * Patients with pelvic or thoracic tumors with an indication for radiotherapy * Patient information and declaration of consent * Patients age ≥ 18 years EXCLUSION CRITERIA * Prior radiotherapy in affected site

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)

FacilityCityRegionStatus
University Medical Center, Departement of Radiation Oncology Göttingen Germany Recruiting
Official registry record

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