Actively Recruiting

Age: 18Years +
All Genders
NCT04085029

Role of Ablative Radiotherapy in the Management of Metastatic Disease: A Patient Data Registry

Led by Duke University · Updated on 2026-02-05

300

Participants Needed

5

Research Sites

518 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Role of Ablative Radiotherapy in the Management of Metastatic Disease: A Patient Data Registry

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 63 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
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Trial Site Locations

Total: 5 locations

1

Duke Cancer Institute Cary

Cary, North Carolina, United States, 27518

Actively Recruiting

2

Durham Veterans Administration Health Care System (DVAHCS)

Durham, North Carolina, United States, 27705

Actively Recruiting

3

Duke University Medical Center

Durham, North Carolina, United States, 27710

Actively Recruiting

4

Duke Women's Cancer Care Raleigh

Raleigh, North Carolina, United States, 27607

Actively Recruiting

5

Duke Raleigh Hospital

Raleigh, North Carolina, United States, 27609

Actively Recruiting

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Research Team

C

Clinical Trials Office

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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