Trials / Enrolling By Invitation
Enrolling By InvitationNCT06723665
The Exploration of 18F-PSMA-1007 PET/CT Imaging in Prostate Cancer Patients
- Status
- Enrolling By Invitation
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- Sponsor
- Affiliated Hospital of Jiangnan University · Academic / Other
- Sex
- Male
- Age
- 40 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
micro-PET imaging showed that 18F-PSMA-1007 had similar or even better pharmacokinetics and imaging performance than 18F-DCFPyL. Due to the convenience of synthesis and good imaging performance, 18F-PSMA-1007 is expected to be popularized in clinical practice.The purpose of this study is to evaluate the performance of 18F-PSMA-1007 in diagnosis, differential diagnosis and efficacy monitoring of prostate cancer.
Detailed description
1. Visual analysis of images: describe the location, size, shape and degree of uptake of lesions; 2. Semi-quantitative analysis: the ratio of lesion site uptake to liver uptake was measured by area of interest method (ROI); 3. Comparative analysis: Compared with clinical routine 18F-FDG PET/CT imaging, the advantages of PSMA PET/CT imaging were clarified; 4. Evaluation and analysis of efficacy: before and after treatment, to clarify the early treatment evaluation value of PSMA PET/CT imaging, and compare it with 18F-FDG PET/CT imaging; 5. Prognostic study: Through multi-factor analysis, the relationship between the level of PSMA PET/CT imaging uptake and the prognosis of patients was clarified.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | 18F-PSMA-1007 | 18F-PSMA-1007 is administered through a superficial dorsal vein, and the patient is given a dose of about 0.1-0.15mCi/kg |
| DRUG | 18F-FDG | 18F-FDG is administered through a superficial dorsal vein, and the patient is given a dose of about 0.1-0.15mCi/kg |
Timeline
- Start date
- 2024-01-25
- Primary completion
- 2026-12-31
- Completion
- 2026-12-31
- First posted
- 2024-12-09
- Last updated
- 2025-01-24
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT06723665. Inclusion in this directory is not an endorsement.