Metastatic Cancer Clinical Trial
Official title:
Role of Ablative Radiotherapy in the Management of Metastatic Disease: A Patient Data Registry
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.
Status | Recruiting |
Enrollment | 1000 |
Est. completion date | September 2029 |
Est. primary completion date | September 2029 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Age = 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: • None |
Country | Name | City | State |
---|---|---|---|
United States | Duke Cancer Institute Cary | Cary | North Carolina |
United States | Duke University Medical Center | Durham | North Carolina |
United States | Durham Veterans Administration Health Care System (DVAHCS) | Durham | North Carolina |
United States | Duke Raleigh Hospital | Raleigh | North Carolina |
United States | Duke Women's Cancer Care Raleigh | Raleigh | North Carolina |
Lead Sponsor | Collaborator |
---|---|
Duke University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Occurrence of acute adverse events following radiotherapy | 90 Days |
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