An Analysis of Urinary Proteases as Biomarkers for Hepatocellular Carcinoma-101423
Completed
- Conditions
- Hepatocellular CarcinomaLiver Disease
- Registration Number
- NCT01316679
- Lead Sponsor
- Vanderbilt University Medical Center
- Brief Summary
Specific urine proteases or groups of these enzymes can be reliable biomarkers and an effective gauge of response to therapy in patients with hepatocellular carcinoma.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 87
Inclusion Criteria
- Ability and willingness to provide written informed consent
- Must be between 18-90 years of age at the time of consent
- Ability to provide urine specimen at protocol-defined timepoints
- Must have treatment interventions planned that are directly related to liver disease (excluding those assigned to group 3-Controls)
Exclusion Criteria
- Suspected inability, e.g. unwillingness to comply with study procedures or unwillingness to provide written consent
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What urinary protease biomarkers correlate with HCC progression and treatment response in NCT01316679?
How do urinary protease profiles compare to standard-of-care diagnostics like AFP for HCC patient monitoring?
Which protease inhibitors or therapeutic targets are validated by NCT01316679's biomarker findings in liver disease?
What adverse events are associated with urinary protease-based biomarker testing in HCC observational studies?
How does NCT01316679's protease research inform non-invasive HCC diagnostics versus competing methods?