Imaging During Surgery in Diagnosing Patients With Prostate, Bladder, or Kidney Cancer
Status: | Not yet recruiting |
---|---|
Conditions: | Prostate Cancer, Cancer, Cancer, Cancer, Bladder Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - 85 |
Updated: | 5/5/2014 |
Start Date: | September 2012 |
Utility of Fluorescence and Photoacoustic Imaging Intraoperatively to Assist With Robotic Assisted Minimally Invasive Surgery
This pilot clinical trial studies imaging during surgery in diagnosing patients with
prostate, bladder, or kidney cancer. New diagnostic imaging procedures, may find prostate,
bladder, or kidney cancer
prostate, bladder, or kidney cancer. New diagnostic imaging procedures, may find prostate,
bladder, or kidney cancer
PRIMARY OBJECTIVES:
I. The primary objective of this pilot study is to assess the ability of fluorescent imaging
and photoacoustic imaging (PAI) in a clinical setting to distinguish benign from malignant
tissue.
SECONDARY OBJECTIVES:
I. To qualitatively determine the possible benefit of PAI and fluorescent imaging over
traditional white light imaging.
OUTLINE:
Patients undergo fluorescence imaging and PAI during robot assisted laparoscopic surgery.
I. The primary objective of this pilot study is to assess the ability of fluorescent imaging
and photoacoustic imaging (PAI) in a clinical setting to distinguish benign from malignant
tissue.
SECONDARY OBJECTIVES:
I. To qualitatively determine the possible benefit of PAI and fluorescent imaging over
traditional white light imaging.
OUTLINE:
Patients undergo fluorescence imaging and PAI during robot assisted laparoscopic surgery.
Inclusion Criteria:
- Patients must have a pathologic confirmation of prostate cancer, bladder cancer, or
kidney cancer based on previous biopsies or procedures OR a strong concern for a
kidney malignancy based on computed tomography (CT) or magnetic resonance imaging
(MRI) imaging
- Ability to understand and the willingness to sign a written informed consent document
Exclusion Criteria:
- Patients with a surgical history or anatomic variant that would preclude robot
assisted laparoscopic approaches to their surgery (i.e. history of ventral hernia
repair with mesh)
- Patients with medical co-morbidities who cannot tolerate laparoscopic surgery
secondary to intra-abdominal carbon dioxide insufflation
- Patients with documented allergy or adverse drug reaction to indocyanine green or
baseline serum creatinine greater than 1.5 mg/dL
We found this trial at
1
site
Stanford University Stanford University, located between San Francisco and San Jose in the heart of...
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