Feasibility Study of Ultrasound Elastography Detecting Prostate Cancer

NACompletedINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

April 11, 2013

Primary Completion Date

June 29, 2015

Study Completion Date

September 18, 2015

Conditions
Prostate Cancer
Interventions
OTHER

Fleet Enema

Since a probe will be introduced into the participant's rectal area, participants will be instructed to give themself one regular Fleet enema.

DEVICE

Aixplorer® ShearWave Elastography (SWE™)

Pre-surgery ultrasound: Aixplorer® ShearWave Elastography (SWE™) Ultrasound System (made by SuperSonic Imagine, Inc.). The device is used transrectally. This device (ultrasound system) has been cleared by the United States Food and Drug Administration (FDA) for the indication for use as described in this consent form.

DIAGNOSTIC_TEST

Pre-surgery Ultrasound

The ultrasound procedure referenced above will be performed at the participant's pre-op visit one to two weeks before their surgery.

PROCEDURE

Prostatectomy

Participants will undergo radical prostatectomy as currently performed at our Moffitt Cancer Center. This procedure is performed under general anesthesia in the operating room. This is considered standard of care.

Trial Locations (1)

33612

H. Lee Moffitt Cancer Center and Research Institute, Tampa

All Listed Sponsors
lead

H. Lee Moffitt Cancer Center and Research Institute

OTHER

NCT03077126 - Feasibility Study of Ultrasound Elastography Detecting Prostate Cancer | Biotech Hunter | Biotech Hunter