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Using 68Ga-PSMA PET-CT multi-parameters to evaluate the efficacy of neoadjuvant therapy for prostate cancer in decision-making in diagnosis and treatment

Using 68Ga-PSMA PET-CT multi-parameters to evaluate the efficacy of neoadjuvant therapy for prostate cancer in decision-making in diagnosis and treatment

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000032215
Enrollment
Unknown
Registered
2020-04-23
Start date
2020-05-01
Completion date
Unknown
Last updated
2020-04-27

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

Conditions

Prostate Cancer

Interventions

Case series:Neoadjuvant therapy

Sponsors

Urology Department, Renji Hospital Affiliated to Shanghai Jiaotong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 45 to 75 years old; 2. good organ function and can metabolize the imaging agent normally; 3. life expectancy >=10 years; 4. no contraindications for radical prostatectomy + expanded lymphadenectomy; 5. Subjects signed an informed consent form prior to enrollment, indicating that they agreed to participate in the study and followed the study procedures

Exclusion criteria

Exclusion criteria: 1. History of other malignant tumors; uncontrolled systemic infection; 2. previous history of imaging agent drug allergies and adverse reactions; 3. vital organs in patients with acute disease progression and parasitic diseases; 4. human immunodeficiency virus (HIV) positive patients, immunodeficiency Patients with sexual diseases, combined immunodeficiency diseases, organ transplants, patients with autoimmune diseases requiring immunosuppressive drugs or steroids, or other severe immunosuppressive states; 5. any mental or cognitive disorders, emotional instability, may restrict understanding, execution, and compliance with the study; 6. other circumstances that the investigator believes are not suitable for participating in this trial.

Design outcomes

Primary

MeasureTime frame
PSA;PI-RADS score;tumor volume;

Secondary

MeasureTime frame
Recist score;TNM stage;pathologic complete response;

Countries

China

Contacts

Public ContactJiahua Pan

Renji Hospital Affiliated to Shanghai Jiaotong University School of Medicine

Jiahua.pan@outlook.com+86 13916989510

Outcome results

None listed

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