Lineberger Comprehensive Cancer Center at University of North Carolina, Chapel Hill
Chapel Hill, North Carolina, 27599, United States
Location status: Recruiting
NCT Number: NCT06306924
The purpose of this registry is to collect clinical data from participants attending UNC Hospitals who present with metastatic cancer and are evaluated to receive radiation therapy as part of their standard of care treatment. The goal of this study is to provide a foundation for studies designed to identify projects across the translational continuum related to metastatic cancer and radiation therapy treatment. The relevant clinical data will be linked to patient-reported outcomes (PROs) thus allowing for a unique and robust dataset. Ultimately, this registry will provide current and future studies with the ability to analyze the correlation of radiation therapy regimens with metastatic cancer outcomes.
Interested in participating?
Request Info18 year and older
All sexes
Observational
Chapel Hill, North Carolina, 27599, United States
Location status: Recruiting
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Written informed consent was obtained to participate in the study and HIPAA
Authorization for release of personal health information. Ability to understand and willingness to sign informed consent
Diagnosed with or is suspected to have metastatic cancer.
Age ≥ 18 years at the time of consent.
Evaluated to receive radiation therapy as part of their standard-of-care treatment plan.
Exclusion criteria
All participants must not meet any of the following exclusion criteria prior to enrollment to participate in this study:
Any serious medical or psychiatric disorder that would interfere with the participant's ability to give informed consent.
Subjects with metastatic cancer receive radiation therapy.
Time frame: Up to 1 month
Clinical data and radiological assessments from participants with metastatic cancer receiving radiation therapy as a part of the standard of care will be collected.
Time frame: Baseline, 1 month, 3 months, 6 months, 9 months, and 12 months
Patient reported outcomes (PRO) from participants will be collected at different time points.
Contact information is provided by the study sponsor or research team.
UNC Lineberger Comprehensive Cancer Center
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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