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NCT03237026Recruiting

Predictive and Prognostic Markers for Treatment Outcomes in Prostate Cancer Patients

Decipher the Biology of Lethal Prostate Cancer-Using Urine Metabolomics and Proteomics Profiling to Search for Predictive and Prognostic Markers for Treatment Outcomes in Prostate Cancer Patients

Source: ClinicalTrials.gov · Last updated 21 Sept 2026

Brief summary (registry, in English)

The study aims to identify potential urine marker metabolites as predictive or prognostic markers for treatment outcomes in patients with prostate cancer.

Status (registry)
Recruiting
Study type
Observational
Enrollment
360 (estimated)
First submitted
30 Jul 2017
Start date
11 Oct 2017
Primary completion date
15 Jan 2027
Lead sponsor
National Taiwan University Hospital
NCT number
NCT03237026

What you commit to

  • Study type: Observational
  • Planned participants: 360
  • From 11 Oct 2017 to the primary completion date, 15 Jan 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Subjects who have other cancers that have not been curatively treated or are disease-free for only 3 years or less. Subjects who have other genitourinary cancers (urothelial, renal cell, etc) are NOT allowed no matter what the disease-free duration is. However, subjects who have been curatively treated and are disease-free for 3 years or longer are allowed to be enrolled.
  • Subjects who have significant infection or inflammation within 8 weeks of the biopsy.

Lab values

  • Subjects who have severe organ function impairment which may significantly alter general cell metabolism or proteomics profiles determined by the investigators, such as Cre \> 3.0, HbA1c \> 9.0%, symptomatic heart failure, or other symptomatic metabolic diseases.

Other

  • Subjects who are taking medicine(s) that may, deemed by the investigators, substantially affect cell metabolism and proteomics profiles.
  • Subjects who have a life expectancy less than 12 months.

Who the study is looking for

  • Subjects who have histopathologically confirmed prostate adenocarcinoma.
  • Subjects who age 30 years to 100 years
  • Subjects who agree to undergo the any of the following four treatments, including radical prostatectomy, definitive prostate radiotherapy, systemic chemotherapy, and androgen deprivation therapy for prostate cancer.
  • Subjects who understand and will comply with the entire study procedures, consent to donate his spot urine (once for 50 ml) for urine metabolomics and proteomic profiling, and agree with subsequent collection and analysis of his clinical information including results of biopsy and the details of treatments and outcomes. (Note: Subjects will be told that the urine metabolomics and proteomics results will not be revealed to them.)

Age in the registry: 30 years to 100 years · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
National Taiwan University
Coordinator of this site? Confirm its status
TaipeiTaiwanRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.