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Non-invasive urine test for cancers

Diagnostic Tools for non-invasive Assessment of Cell Phenotypes and Cancer from Patient fluids

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-SPD-17011540
Enrollment
Unknown
Registered
2017-06-01
Start date
2017-06-01
Completion date
Unknown
Last updated
2017-06-05

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

Conditions

Nasopharyngeal Cancer, Breast Cancer, Gastric Cancer, Colorectal Cancer

Interventions

Population:Nil

Sponsors

Entopsis Asia
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 85 Years

Inclusion criteria

Inclusion criteria: The first phase will be to examine urine samples obtained from patients with primary forms of cancer (untreated) and age matched controls ranging from 20-85. Depending on the screening criteria, patients who have been treated will be included in the screening procedure to determine if the platform can detect recurrence. As this platform is proposed for use with multiple forms of cancer, the inclusion criteria will be similar/identical among all patients. The cancers to be tested include 1) Lung and Bronchus; 2) Stomach; 3) Breast; 4) Esophagus; 5) Liver; 6) Colorectum; 7) Prostate; and 8) other cancers depending on disease prevalence and clinical access. 1. Patients must be >20 years of age; 2. Patients should have untreated, diagnosed forms of cancer (patients include newly diagnosed cancers and relapses greater than 6 months since the last intervention); 3. Patents must be mentally competent to make informed consent; 4. Patients must provide written informed consent and be willing to comply with the requirements of the protocol.

Exclusion criteria

Exclusion criteria: 1. Inability to provide informed consent; 2. Concurrent use or receipt within the previous 5 months of any chemo-therapeutic drugs or irradiation to treat the cancer, or treatment with corticosteroids at a dose > 40 mg/day (Note: doses <40 mg/day are permitted and not considered to be an exclusion factor); 3. Serious cardiovascular disease under current treatment; 4. Untreated type I and II diabetes; 5. Urine glucose levels above 1.0 mmol/L, which may be indicative of other underlying diseases; 6. Serious infections (hospitalization) within the prior 3 months.

Design outcomes

Primary

MeasureTime frame
Molecular binding profile on NuTECs of molecules present in patient urine.;

Countries

China

Contacts

Public ContactKenneth R. Boheler

Hong Kong University

bohelerk@hku.hk+852 2831 5405

Outcome results

None listed

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