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68Ga-PSMA PET/MRI in Conjunction With mpMRI for Evaluating Prospective Prostate Cancer Risk

Utilizing 68Ga-PSMA PET/MRI Imaging in Conjunction With mpMRI for Evaluating Prospective Prostate Cancer Risk

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06494696
Enrollment
71
Registered
2024-07-10
Start date
2024-07-01
Completion date
2027-05-31
Last updated
2024-07-10

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

Conditions

Prostate Cancer

Keywords

Ga-68 PSMA PET/MRI, PI-RADS, Biopsy naive

Brief summary

The goal of this observational study is to learn if Ga-68 PSMA PET/MRI can better diagnose prostate cancer than mpMRI in males between 40 to 85 years old who is naive to prostate biopsy and is suspicious for prostate cancer by elevated PSA or lower urinary tract symptoms. The main questions it aims to answer are: 1. Does PSMA PET/MRI have better PPV and NPV than mpMRI to diagnose prostate cancer? 2. Does lesion location concordance in PSMA PET and MRI effect diagnosis accuracy? Participants will: 1. Undergo a Ga-68 PSMA PET/MRI scan and keep followed up for 2 years to check if prostate cancer is diagnosed after the scan. 2. Between the follow-up period, visit the clinic once every 6 months for checkups and blood tests.

Interventions

DIAGNOSTIC_TESTGa-68 PSMA PET/MRI

The participant will undergo a Ga-68 PSMA PET/MRI scan, and then be followed up for 2 years to see if prostate cancer is diagnosed.

Sponsors

National Science and Technology Council
CollaboratorFED
Chang Gung Memorial Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
40 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

1. Patients who indicated MRI of pelvis due to clinical suspicion of prostate cancer based on elevated PSA (4\ 20 ng/mL), abnormal digital rectal examination or lower urinary tract syndromes. 2. Males aged between 40 and 85 years with a life expectancy greater than two years. 3. Naïve to prostate biopsy in the past. 4. Assessment of daily physical status graded 0 to 2 based on the Eastern Cooperative Oncology Group (ECOG) criteria. 5. Willing to sign the informed consent.

Exclusion criteria

1. Unable to tolerate the PET/MRI scan, such as those with claustrophobia, unable to lie still, consciousness unclear, vital sign unstable, or having MRI unsafe metallic implants or devices. 2. With renal impairment (glomerular filtration rate lower than 30 ml/min/1.73 m2), and allergy to medium contrast. 3. High risk to conduct examination after evaluations of PI 4. Patient had previous malignancy history

Design outcomes

Primary

MeasureTime frameDescription
PPV of concordant PET/MRI lesion plus PI-RADS score 4~52 years after PSMA PET/MRI scanComparing positive predictive values (PPV) of using concordant PET/MRI lesion plus PI-RADS score 4\ 5 as positive test with PPV of using PI-RADS 4\ 5 alone as positive test to predict diagnosing prostate cancer within 2 years.
NPV of using negative PET lesion plus PI-RADS score 1~32 years after PSMA PET/MRI scanComparing negative predictive values (NPV) of using negative PET lesion plus PI-RADS score 1\ 3 as negative test with NPV of using PI-RADS 1\ 3 alone as negative test to predict diagnosing prostate cancer within 2 years.

Countries

Taiwan

Contacts

Primary ContactJing-Ren Tseng, MD
drTsengJR@gmail.com+886-975361314

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026