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Clinical Translational Research of 68Ga/18F-PSMA in Oncological Imaging

Clinical Translational Research of 68Ga/18F-PSMA in Oncological Imaging

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100050105
Enrollment
Unknown
Registered
2021-08-16
Start date
2021-08-16
Completion date
Unknown
Last updated
2022-04-25

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

Conditions

Malignancy

Interventions

Gold Standard:biopsy or surgical pathological diagnosis
Index test:68Ga/18F-PSMA

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients with high suspicion of prostate cancer: (1) The serum PSA value has changed compared with the previous one (when PSA0.35ng/mL, or the annual change is >0.75ng/mL when PSA>4.0ng/mL); (2) First- and second-degree relatives with a history of prostate cancer; (3) For patients with nuclear magnetic resonance PI-RADS score >= 3 or prostate cancer confirmed by biopsy or surgical pathology, clinical laboratory test results (blood routine, biochemistry, serum PSA) within one month before PET/CT examination can be provided ; there are at least two other imaging examinations including CT, MRI, nuclear medicine, ultrasound and other imaging techniques; the examination can be completed independently. 2. For patients with breast cancer, kidney cancer, thyroid cancer, colorectal cancer and other malignant tumors who have been diagnosed, the clinical laboratory test results (blood routine and biochemistry) within one month before the PET/CT examination can be provided; there are at least two other imaging examinations including CT, MRI, nuclear medicine, ultrasound and other imaging techniques; the examination can be completed independently. 3. Patients can fully understand and voluntarily participate in this trial, and sign the informed consent.

Exclusion criteria

Exclusion criteria: There is a history of other malignancies.

Design outcomes

Primary

MeasureTime frame
Sensitivity;Specificity;Positive Predictive Value;Negative Predictive Value;Accuracy;

Countries

China

Contacts

Public ContactFan Yan

Peking University First Hospital

fanyan980618@sina.com+86 10 83572791

Outcome results

None listed

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