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Clinical Translational Research of 68Ga/18F/99mTc-P137 in Oncological Imaging

Clinical Translational Research of 68Ga/18F/99mTc-P137 in Oncological Imaging

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100049791
Enrollment
Unknown
Registered
2021-08-09
Start date
2021-08-10
Completion date
Unknown
Last updated
2022-04-19

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

Conditions

Malignancy

Interventions

Gold Standard:Pathological diagnosis
Index test:68Ga/18F/99mTc-P137

Sponsors

Nuclear Medicine Department,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) Changes in serum PSA values compared with previous ones (when PSA0.35ng/mL, or PSA>4.0ng/mL annual change> 0.75ng/mL); (2) first- and second-degree relatives with a history of prostate cancer; (3) nuclear magnetic resonance PI-RADS score >= 3) or patients with prostate cancer confirmed by biopsy or surgical pathology, PET can be provided /Clinical laboratory test results (blood routine, biochemistry, serum PSA) within one month before CT examination; at least two other imaging examinations including CT, MRI, nuclear medicine, ultrasound and other imaging techniques; can be completed independently an examination; 2. Patients who have been diagnosed with breast cancer, kidney cancer, thyroid cancer, colorectal cancer and other malignant tumors can provide clinical laboratory test results (blood routine, biochemistry) within one month before the PET/CT examination; at least include CT, Two other imaging examinations including MRI, nuclear medicine, ultrasound and other imaging techniques; can complete the examination independently; 3. The test 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 malignant tumors; those who cannot cooperate.

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