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Search / Trial NCT04723810

TumorGlow Intraoperative Molecular Imaging (IMI)

Launched by UNIVERSITY OF PENNSYLVANIA · Jan 20, 2021

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

ClinConnect Summary

The TumorGlow Intraoperative Molecular Imaging (IMI) trial is a research study designed to help doctors better see and treat solid tumors during surgery. This study is looking at how safe and effective a special imaging technique using a dye called indocyanine green is when used to guide surgeons in removing tumors. It is open to adults aged 18 and older who have solid tumors or diseased tissue that can be surgically removed and are at risk of returning after surgery. To be eligible, patients must be in good health for surgery and capable of understanding the consent process.

If you participate in this trial, you can expect to have your surgery with the assistance of this new imaging method, which could help improve the chances of removing all of the tumor while minimizing the risk of recurrence. It’s important to note that individuals who are pregnant, children, or those with certain health issues, such as uncontrolled high blood pressure or allergies to iodide, cannot take part in the study. The trial is currently recruiting participants, and your doctor can provide more information about whether this study is a good fit for you or your loved one.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Adult patients 18 years of age or older.
  • Patients presenting with any solid tumor and/or diseased tissue even benign nodules presumed to be resectable and at risk for recurrence on pre-operative assessment.
  • Good operative candidate as determined by the treating physician and/or multidisciplinary team.
  • Subject capable of giving informed consent.
  • Exclusion Criteria:
  • Subject unable to participate in the consent process.
  • Vulnerable population including pregnant women, prisoners, and children.
  • History of uncontrolled hypertension (e.g., history of an ER admission for hypertensive crisis or ≥ 3 blood pressure medications)
  • Patients with a self-reported history of iodide allergies.

About University Of Pennsylvania

The University of Pennsylvania, a prestigious Ivy League institution located in Philadelphia, is renowned for its commitment to advancing medical research and improving healthcare outcomes. As a clinical trial sponsor, the university leverages its extensive resources, interdisciplinary expertise, and cutting-edge facilities to conduct innovative studies across various therapeutic areas. With a focus on translating scientific discoveries into clinical applications, the University of Pennsylvania fosters collaborations among leading researchers, clinicians, and industry partners, ensuring rigorous trial design and adherence to ethical standards. Through its dedication to excellence in research and education, the university plays a pivotal role in shaping the future of medicine.

Locations

Philadelphia, Pennsylvania, United States

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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