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NCT07533344Completed

Ga-68 PSMA PET/CT vs mpMRI in Cognitive Prostate Biopsy

Comparison of Ga-68 PSMA PET/CT and Multiparametric Prostate MRI for Lesion Detection in Cognitive Prostate Biopsy

Source: ClinicalTrials.gov · Last updated 16 Apr 2026

Brief summary (registry, in English)

Prostate cancer is the most common malignancy among elderly men. With the routine use of prostate-specific antigen (PSA) testing since the 1980s, the incidence of prostate cancer has significantly increased. The diagnosis of prostate cancer is established through prostate biopsy, and several biopsy techniques have been developed in recent years. Prostate biopsy can be broadly classified into systematic and targeted biopsy techniques. Systematic biopsy is performed under transrectal or transperineal ultrasound guidance without the use of prior imaging. Targeted biopsy techniques include cognitive biopsy, multiparametric magnetic resonance imaging (mpMRI) fusion biopsy, in-bore MRI biopsy, and robotic biopsy. Cognitive biopsy is defined as the targeting of lesions identified on pre-biopsy imaging, usually multiparametric prostate MRI. MRI-fusion biopsy integrates mpMRI images with real-time ultrasound images, while in-bore biopsy is performed directly under MRI guidance. Although MRI-fusion biopsy is considered the gold standard technique, cognitive biopsy is more commonly used in developing countries due to lower cost and reasonable diagnostic accuracy. Recently, Ga-68 prostate-specific membrane antigen (PSMA) PET/CT has become the gold standard imaging modality for staging prostate cancer after receiving FDA approval. PSMA is a type II transmembrane protein highly expressed on prostate cancer cells. PSMA PET/CT has high sensitivity and specificity for the detection, staging, and recurrence of prostate cancer. Currently, multiparametric prostate MRI is commonly used to detect lesions before cognitive biopsy. However, there is no study in the literature evaluating the use of PSMA PET/CT imaging for guiding cognitive prostate biopsy. In this retrospective single-center study, the investigators aim to compare the effectiveness of Ga-68 PSMA PET/CT and multiparametric prostate MRI as imaging modalities used prior to cognitive prostate biopsy.

Status (registry)
Completed
Study type
Observational
Enrollment
60 (actual)
First submitted
7 Apr 2026
Start date
1 Aug 2025
Primary completion date
1 Feb 2026
Lead sponsor
Fatih Sultan Mehmet Training and Research Hospital
NCT number
NCT07533344

What you commit to

  • Study type: Observational
  • Participants enrolled: 60
  • From 1 Aug 2025 to the primary completion date, 1 Feb 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Patients with incomplete clinical or imaging data
  • Patients without available histopathological biopsy results
  • Patients who underwent prostate biopsy without pre-biopsy imaging
  • Patients with lesions scored PIRADS ≤3 on multiparametric prostate MRI

Who the study is looking for

  • Male patients aged 40 years or older
  • Patients who underwent cognitive prostate biopsy between 2020 and 2024
  • Patients who had pre-biopsy imaging with multiparametric prostate MRI or Ga-68 PSMA PET/CT
  • Patients with available prostate biopsy pathology results
  • Patients with prostate lesions scored PIRADS 4 or 5 on multiparametric prostate MRI

Age in the registry: 40 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Fatih Sultan Mehmet Training and Research Hospital
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.