Role of Ablative Radiotherapy in the Management of Metastatic Disease: A Patient Data Registry
Recruiting
- Conditions
- OligometastasisMetastatic Cancer
- Registration Number
- NCT04085029
- Lead Sponsor
- Duke University
- Brief Summary
The purpose of this study is to provide a registry of participants in order to assess the acute adverse event rates following ablative radiotherapy for metastatic disease.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 300
Inclusion Criteria
- Age β₯ 18 years of age
- Radiographic evidence of metastatic disease (may include oligoprogression, oligorecurrence or oligometastasis) at the time of study enrollment
- Planned to receive, currently receiving, or have completed hypofractionated image guided radiotherapy (ablative radiotherapy) to an extracranial site(s)
- Patient must sign study-specific informed consent
Exclusion Criteria
β’ None
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Occurrence of acute adverse events following radiotherapy 90 Days
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (5)
Duke Cancer Institute Cary
πΊπΈCary, North Carolina, United States
Durham Veterans Administration Health Care System (DVAHCS)
πΊπΈDurham, North Carolina, United States
Duke University Medical Center
πΊπΈDurham, North Carolina, United States
Duke Women's Cancer Care Raleigh
πΊπΈRaleigh, North Carolina, United States
Duke Raleigh Hospital
πΊπΈRaleigh, North Carolina, United States
Duke Cancer Institute CaryπΊπΈCary, North Carolina, United StatesTaylor Fryman, BS CHESContact919-668-3726Taylor.Fryman@duke.edu