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RecruitingNCT06306924Updated May 6, 2026

UNC Metastatic Cancer Radiation Therapy Registry

An observational study in Cancer and Metastatic Cancer, sponsored by UNC Lineberger Comprehensive Cancer Center. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-05-06.

Sponsored by UNC Lineberger Comprehensive Cancer Center · Observational

From the registry’s dates

  • Started Apr 2024; still recruiting 2 years 5 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
2,000
Ages
18 Years and older
Sex
All
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Study summary

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.

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Conditions studied

  • Cancer
  • Metastatic Cancer

Keywords

  • radiation therapy
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In context

Neoplasms

9,365 studies on the registry are indexed under Neoplasms; 2,489 are open to participants now.

This study's planned enrollment of 2,000 is above the median of 204 across 1,683 observational studies indexed under Neoplasms.

Browse Neoplasms studies →

Lead sponsor

UNC Lineberger Comprehensive Cancer Center is the lead sponsor of 414 studies on the registry; 96 are open to participants now.

Of its 32 completed or terminated interventional studies of FDA-regulated products, 25 (78%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Subjects with metastatic cancer receiving palliative radiation therapy at the University of North Carolina Chapel Hill.

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

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.

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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
2,000 participants (estimated)
Patient registry
No

Groups and cohorts

  • Palliative radiation therapy

    Subjects who are with metastatic cancer receive palliative radiation therapy.

    Radiation: Radiation therapy

Interventions

  • RadiationRadiation therapy

    Subjects with metastatic cancer receive radiation therapy.

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What researchers measure

Primary outcomes

  1. Clinical Data

    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: Up to 1 month

Secondary outcomes

  1. Patient reported outcomes (PRO)

    Patient reported outcomes (PRO) from participants will be collected at different time points.

    Time frame: Baseline, 1 month, 3 months, 6 months, 9 months, and 12 months

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Study locations

1 of 1 sites recruiting
  • Lineberger Comprehensive Cancer Center at University of North Carolina, Chapel Hill
    Chapel Hill, North Carolina 27599, United States
    Recruiting
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References and documents

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 6, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06306924
Lead sponsor
UNC Lineberger Comprehensive Cancer Center
Responsible party
Sponsor
First posted
Mar 12, 2024
Start date
Apr 21, 2024
Primary completion
May 2033 (estimated)
Completion
May 2033 (estimated)
Last update
May 6, 2026

Study contacts

Kadiata Toumbou
Contact
kadiata@email.unc.edu
(202) 569-3721
Victoria Xu
Contact
victoria_xu@med.unc.edu
Shivani Sud, MD
principal investigator · UNC Lineberger Comprehensive Cancer Center

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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