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Study on molecular markers of prostate cancer metastasis tropism

Study on molecular markers of prostate cancer metastasis tropism

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400089922
Enrollment
Unknown
Registered
2024-09-19
Start date
2024-01-03
Completion date
Unknown
Last updated
2024-09-23

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

Conditions

Prostate Cancer

Interventions

bone metastases:NA
lymphatic metastasis:NA
Both Bone and lymphatic metastasis:NA
none of metastasis:NA

Sponsors

Shanghai Changhai Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: (1) Male gender, (2) Expected lifespan =5 years; (3) Patients diagnosed with prostate cancer confirmed by biopsy prior to enrollment; (4) Patients with detailed and accurate recent reports of whole-body Magnetic Resonance Imaging (MRI) and whole-body Bone Scan (ECT) or Positron Emission Tomography/Computed Tomography (PET/CT), capable of determining whether the prostate cancer has metastasized and the specificity of the metastasis; (5) Willingness to accurately complete subject survey questionnaires; (6) Willingness to participate in long-term follow-up; (7) The patient himself or a direct relative authorized by the patient has signed the clinical trial informed consent form. Participants who meet all the inclusion criteria can be included in the study analysis.

Exclusion criteria

Exclusion criteria: (1) Concurrent other malignancies; (2) Recent radiation therapy, chemotherapy, or other treatments that could affect plasma samples; (3) Presence of other significant diseases that could interfere with study results, such as severe heart, liver, or kidney dysfunction; (4) Currently using or having recently used drugs that could affect the results of molecular biological analyses; (5) Presence of severe coagulation disorders or other hematologic diseases; (6) Poor compliance, unable to follow the study schedule. Participants meeting any one of the exclusion criteria will be excluded from the study.

Design outcomes

Primary

MeasureTime frame
Furin expression;PLS3 expression;

Countries

China

Contacts

Public ContactYang Chenghua

Changhai Hospital

chenghua-yang@qq.com+86 136 1177 9405

Outcome results

None listed

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