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A single-center, prospective, head-to-head comparative study of the diagnostic efficacy of 18F-PSMA PET/CT and 18F-PSMA PET/MR for primary and metastatic prostate cancer

A single-center, prospective, head-to-head comparative study of the diagnostic efficacy of 18F-PSMA PET/CT and 18F-PSMA PET/MR for primary and metastatic prostate cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400094962
Enrollment
Unknown
Registered
2024-12-31
Start date
2025-01-01
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Prostate cancer

Interventions

Gold Standard:All cases were verified by surgical resection, biopsy histopathological results or clinical follow-up data. Lesions that were difficult to obtain histopathology (such as bone metastasis,
2.After anti-tumor treatment, the imaging follow-up showed that the lesion volume was reduced or disappeared. The follow-up time was 3 to 15 months (median follow-up time was 7 months).
Index test:1. Main observation points: Comparison of the number of lesions detected by the two examinations: Comparison of the number of lesions detected by 18F-PSMA PET/CT and 18F-PSMA PET/MR for pri

Sponsors

Yunnan cancer hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1.Patients with clinical suspicion of prostate cancer or recurrence of prostate cancer after treatment. 2.Patients without contraindications to PET/CT and PET/MR examinations. 3.Complete clinical pathological and imaging data. 4.Signed informed consent to accept 18F-PSMA-1007 PET/CT and PET/MR examinations.

Exclusion criteria

Exclusion criteria: 1.Patients who cannot tolerate the test or have contraindications to the test. 2.Patients with other primary malignant tumors. 3.Patients with other diseases that cause lymphadenopathy. 4.Patients who do not accept biopsy and regular follow-up.

Design outcomes

Primary

MeasureTime frame
mMaximum standardized uptake value(SUVmax);Number of lesions;Pathological or follow-up results;Prostate Specific Antigen(PSA);

Countries

China

Contacts

Public ContactLong Chen

Yunnan cancer hospital

lonechen1983@hotmail.com+86 152 8826 3130

Outcome results

None listed

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