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Multi-center study of Benign Prostate Hyperplasia Fluid Biomarker Investigation (BPH-FBI)

Multi-center study of Benign Prostate Hyperplasia Fluid Biomarker Investigation (BPH-FBI)

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400090699
Enrollment
Unknown
Registered
2024-10-11
Start date
2024-11-01
Completion date
Unknown
Last updated
2025-04-14

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

Conditions

Prostatic Hyperplasia

Interventions

Healthy control group:None

Sponsors

Shanghai Ninth People’s Hospital, Shanghai Jiaotong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 90 Years

Inclusion criteria

Inclusion criteria: Benign Prostatic Hyperplasia (BPH) Group: 1. Patients aged 50 years or older. 2. Presence of clear symptoms of prostatic hyperplasia, meeting the diagnostic criteria for BPH. 3. Subjects fully understand the patient information, agree to adhere to the study procedures, and sign the informed consent form. Healthy Control Group: 1. No history of malignant tumors. 2. No history of prostate-related diseases. 3. No significant underlying diseases. 4. Subjects fully understand the patient information, agree to adhere to the study procedures, and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. History of malignant tumors; 2. Patients with a history of significant underlying diseases.

Design outcomes

Primary

MeasureTime frame
PI-RADs score of Enhanced MRI of the prostate;

Secondary

MeasureTime frame
Max Urine flow rate (Qmax);Prostate-specific antigen;International prostate symptom score;

Countries

China

Contacts

Public ContactXu Bin

Shanghai Ninth People’s Hospital, Shanghai Jiaotong University School of Medicine

chxb2004@126.com+86 133 8627 1601

Outcome results

None listed

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