Prostate biopsy is the definitive test to establish the diagnosis of prostate cancer. The standard of care biopsy needles do not predictably obtain full cores of tissue and what tissue obtained is often fragmented, making pathologic review a challenge. The VMCore Biopsy System has a geometry in the tip of its biopsy needles that capture more tissue in a single sample. This study is to compare the characteristics of tissue captured by either standard of care needles and the VMCore needle.
This post-market study is being conducted in order to assess the capability of the VMCore biopsy needle to capture prostate tissue in subjects consenting to the use of both the VMCore needle and the urological practice's standard of care needle for twinned samples during a routine prostate biopsy procedure. The primary endpoints are to success in tissue core sampling, safety of the sampling, and subject's tolerance to the procedure.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
40
Prostate Examine
Prostate Examine
Georgia Urology
Cartersville, Georgia, United States
RECRUITINGProcedure Success
Percentage of tissue samples suitable for pathological review
Time frame: 1 Day of the procedure
Adverse Events
Incidence and Severity of Adverse events associated with use of the biopsy needles
Time frame: 1 Day of the procedure
Patient Pain During use of the biopsy needles
Pain measured with Likert Scale of 1 to 5
Time frame: 1 Day of the procedure
Mean Tissue volume for each sample taken
Length and diameter of tissue samples for cubic centimeters of volume
Time frame: 1 Day of the procedure
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.