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Study identifier: NCT06907446 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: Prostate Cancer  ·  Sponsor: University of California, Davis

PhaseNA
Planned participants50
Who can joinMale, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Marc Dall'Era, MD  ·  916-734-2893  ·  mdallera@ucdavis.edu

Elisa Lee  ·  916-734-5173  ·  elilee@ucdavis.edu

Always discuss trial participation with your own doctor first.

Locations (1)

UC Davis Departments of Urologic OncologySacramento, California, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06907446