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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04085029
Other study ID # Pro00103137
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 26, 2019
Est. completion date September 2029

Study information

Verified date March 2024
Source Duke University
Contact Taylor Fryman, BS CHES
Phone (919) 668 3726
Email Taylor.Fryman@duke.edu
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial 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.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Locations

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

Sponsors (1)

Lead Sponsor Collaborator
Duke University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Occurrence of acute adverse events following radiotherapy 90 Days
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