Condition: Cancer · Solid Malignant Tumors · SCC - Squamous Cell Carcinoma · Sponsor: Vanderbilt-Ingram Cancer Center
Imaging will be exploratory and be used intraoperatively. There have been no discovered risks associated with the device to be used in this study, and none are anticipated given the diagnostic and non-invasive, 'ex vivo' nature of device use. Of note, the surgical resection will proceed as per standard of care and will not be affected by the research protocol. Potential Benefit: Imaging intra-operatively will ensure surgeons to identify at risk resection margins. Time Commitment: There are no additional visits that will be asked of you to partake in this study. Drug is FDA approved and Exposure to Radiation is minimal.
This description comes directly from the study's public registry record.
Nicole Jones · 615-936-2807 · nicole.l.jones@vumc.org
Kyrionna Golliday · 615-421-1585 · kyrionna.m.golliday@vumc.org
Always discuss trial participation with your own doctor first.
| Vanderbilt University Medical Center | Nashville, Tennessee, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06915454