Contrast Enhanced Intraoperative Ultrasound for Detection and Characterization of Renal Mass Undergoing Open Partial Nephrectomy
Completed · Not applicable
Conditions studied: Kidney Cancer
In brief
The goal of this clinical research is to learn how effective an ultrasound contrast agent, called DEFINITY, is when used during ultrasound-guided surgery to remove part of one or both kidneys.
Key facts
- Study ID
- NCT01894607
- Run by
- M.D. Anderson Cancer Center
- People needed
- 11
- Starts
- 2013-10-01
- Last updated by the study team
- 2016-04-14
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients must have previous cross sectional imaging (CT or MRI) demonstrating renal mass or masses that is amenable to open partial nephrectomy.
- Patient is scheduled for intraoperative ultrasound guided open partial nephrectomy.
- Patient must sign informed consent, with risks and benefits of CEUS explained (see risks outlined on the following pages)
You may not qualify if…
- Patients with known renal mass scheduled for total or laparoscopic partial nephrectomy.
- Patients who are hypersensitive to Definity (Perflutren Lipid Microsphere)
- Patients with known history of right-to-left, bidirectional or transient right-to-left cardiac shunts.
- Pediatric patients less than 18 years of age.
- Pregnant or nursing mothers.
Where it is running
- University of Texas MD Anderson Cancer Center — Houston, Texas, United States
Full record on ClinicalTrials.gov
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