Kidney Cancer Clinical Trial

Registration and Fusion of Real-Time Ultrasound With CT for Lesion Localization and Characterization

Summary

Acquire CT data and US and transducer position data (magnetic sensor system) of focal hepatic or renal lesions to serve as sample data sets for fusion algorithm development and subsequent optimization.

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Full Description

Acquire CT data and US and transducer position data (magnetic sensor system) of focal hepatic or renal lesions to serve as sample data sets for fusion algorithm development and subsequent optimization.

Optimize image fusion algorithms for use in goal. Develop registration algorithms that result in maximal lesional overlap with a clinically relevant difference in an epicenter location of ≤ 2 cm for lesional identification and, ultimately ≤ 0.3 cm for interventional procedures.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Focal lesion involving the liver or kidney bases on CT or MRI Imaging
Liver lesion size >5 mm and <5 cm in diameter or renal lesion size is >5 mm and <4 cm in diameter
Age >18 years old
Patient has provided written informed consent

Exclusion Criteria:

Patient with cardiac pacemaker or defibrillator
Pregnant or lactating woman
Patient with severe IV contrast allergy (previous reaction to IV contrast not mitigated by appropriate premedication)
Patient unable to give informed consent

Study is for people with:

Kidney Cancer

Estimated Enrollment:

80

Study ID:

NCT00586235

Recruitment Status:

Completed

Sponsor:

Mayo Clinic

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There is 1 Location for this study

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Mayo Clinic
Rochester Minnesota, 55905, United States

How clear is this clinincal trial information?

Study is for people with:

Kidney Cancer

Estimated Enrollment:

80

Study ID:

NCT00586235

Recruitment Status:

Completed

Sponsor:


Mayo Clinic

How clear is this clinincal trial information?

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