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MRI/ultrasound fusion-guided prostate needle biopsy

MRI/ultrasound fusion-guided prostate needle biopsy - MRI/ultrasound fusion-guided prostate needle biopsy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000044363
Enrollment
50
Registered
2021-06-01
Start date
2021-06-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate cancer

Interventions

Perform a transperineal prostate needle biopsy the day after admission.

Sponsors

Nagoya University Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Patients with localized prostate cancer with a serum PSA level of >4.0 ng / mL and <20 ng / ml, suspected of having Significant cancer by MRI.

Exclusion criteria

Exclusion criteria: Exclude patients who do not meet the above eligibility criteria. Patients who have difficulty inserting a transrectal ultrasound probe due to anal stenosis. Diabetic patients who are positive for urinary ketone bodies, have fasting blood glucose of 200 mg / dL or higher, and have postprandial blood glucose of 300 mg / dL or higher. Patients with a foci of infection in the perineum, which is the puncture site. Patients with lesions of a diameter of 10 mm or more on MRI which detected on transrectal ultrasonography and judged to be easy to biopsy by urologist.

Design outcomes

Primary

MeasureTime frame
Detection rate of Significant Cancer in transperineal prostate needle biopsy by Biojet system

Countries

Japan

Contacts

Public ContactTakashi Fujita

Nagoya University Graduate School of Medicine Urology

tfujita@med.nagoya-u.ac.jp052-744-2984

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026