Back to Trials
NCT06907446NARecruiting

Comparison of New SUREcore Biopsy of Needle to Standard of Care During Transperineal Prostate Biopsies

University of California, Davis

Start Date

5/1/2025

Completion Date

12/1/2027

Summary

To study a novel biopsy needle system for performing transperineal prostate biopsy. Prostate biopsy remains the standard approach for prostate cancer detection. While pre-biopsy MRI allows for targeting of visible lesions, systemic or 'off target' samples are recommended due to the well-recognized risk of undegrading and under sampling with current commercially available needles. The SureCore plus single-use biopsy needle produces a more intact tissue core with a same caliber 18g needle with \~21% more tissue per core in pre-clinical studies. This research study will determine if a new biopsy needle designed to produce more robust tissue cores per sample can improve detection and characterization of prostate cancer.

Eligibility Criteria

Age Range: 18 years to No maximum

Inclusion Criteria: * Patient older than age of 18 undergoing prostate biopsy Exclusion Criteria: * Unable to consent * Any comorbidity that, in the opinion of the investigator, could compromise protocol objectives * Prisoners

Interventions

DIAGNOSTIC_TEST

Comparison of Biopsy Needle Types for Prostate Biopsy

Interested in This Trial?

Contact the trial locations directly using the information below to learn more about enrollment.

Expressing interest lets you review the study and consent before we connect you with the research site.

Conditions

Prostate Cancer

Locations

UC Davis Departments of Urologic Oncology

Sacramento, California 95817

United States