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Diagnostic Efficacy of Prostate Targeted, Perilesional, and Systematic Biopsy: A Prospective Randomized Controlled Trial

Diagnostic Efficacy of Prostate Targeted, Perilesional, and Systematic Biopsy: A Prospective Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116504
Enrollment
Unknown
Registered
2026-01-12
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Prostate Cancer

Interventions

Experimental group:In addition to targeted biopsy combined with systematic biopsy, perilesional biopsy is performed around the index lesion.
Control group:None

Sponsors

Northern Jiangsu People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Serum prostate-specific antigen (PSA) level > 4 ng/mL; 2. Prostate lesion with a Prostate Imaging Reporting and Data System (PI-RADS) version 2.1 score of =4, or a clearly suspicious lesion assigned a PI-RADS score of 3 on multiparametric MRI; 3. Patient scheduled to undergo or has undergone prostate biopsy;

Exclusion criteria

Exclusion criteria: 1. Contraindications to prostate biopsy; 2. Prior history of prostate biopsy; 3. Previous treatment with androgen deprivation therapy (ADT) or pelvic radiotherapy; 4. History of transurethral resection of the prostate (TURP).

Design outcomes

Primary

MeasureTime frame
csPCa rate;

Secondary

MeasureTime frame
Positive rate;The rates of pathological up-regulation and down-regulation after radical treatment;

Countries

China

Contacts

Public ContactXuefei Ding

Northern Jiangsu People's Hospital

mn103ding@163.com+86 180 5106 1234

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026