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A Project to Improve the Clinical Management of Individualized Treatment of Metastatic Prostate Cancer through the Analysis of the Current Situation of mHSPC Diagnosis and Treatment and Genetic Testing in China

A Project to Improve the Clinical Management of Individualized Treatment of Metastatic Prostate Cancer through the Analysis of the Current Situation of mHSPC Diagnosis and Treatment and Genetic Testing in China

Status
Recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300073600
Enrollment
Unknown
Registered
2023-07-16
Start date
2022-10-30
Completion date
Unknown
Last updated
2023-07-16

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

Conditions

prostate cancer

Interventions

observational study:non-interventional

Sponsors

Chinese PLA general hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Men aged = 18 years and < 75 years. (2) Histologically or cytologically confirmed prostate cancer; (3) Eastern Cooperative Oncology Group (ECOG) performance status score = 1, life expectancy = 10 years; (4) No other cancer chemotherapy history, no chemotherapy, no endocrine therapy contraindications. (5) The subjects voluntarily participate, and the subjects themselves must sign the informed consent form (ICF), indicating that they understand the purpose of this study and the required procedures, and are willing to participate in the study. Subjects must be willing and comply with prohibitions and restrictions specified in the study protocol.

Exclusion criteria

Exclusion criteria: (1) Prostate pathology shows neuroendocrine prostate cancer, including small cell carcinoma. (2) Other situations where the investigator considers as inappropriate for the subjects to participate in this study.

Design outcomes

Primary

MeasureTime frame
Time to mCRPC;

Countries

China

Contacts

Public ContactWang Baojun

Chinese PLA general hospital

13521908910@126.com+86 135 2190 8910

Outcome results

None listed

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