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Clinical trial of colon cancer diagnostic reagent by blood mRNA examination for practical use

Clinical trial of colon cancer diagnostic reagent by blood mRNA examination for practical use - Clinical trial of colon cancer diagnostic pharmaceutical by blood mRNA examination

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000018914
Enrollment
200
Registered
2015-09-04
Start date
2015-12-27
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

colon cancer

Interventions

None listed

Sponsors

Kanazawa University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who meet the criteria below will be enrolled. Gender, admission/outpatient clinic will not be assessed. 1) Patients who undergo total colonoscopy examination 2) Patients aged more than 20 years when informed consent is obtained. 3) Patients who give the informed consent. Colon cancer 100 patients and non-colon cancer 100 cases will be enrolled.

Exclusion criteria

Exclusion criteria: The patients who meet any of the criteria below will be excluded. 1) Patients who have been diagnosed with malignancy within 5 year of the date of the informed consent. 2) Patients who have been treated with interferon treatment within one year of the date of the informed consent, or is currently undergoing interferon treatment. 3) Patients who have been treated with adrenal hormone (except for local treatment) or biological drug (etc. infliximab) within 6 months. 4) Patients who have been treated with anti-cancer drug within 6 months of the informred consent. 5) Patients who are infected with hepatitis B, hepatitis C or other infectious diseases. 6) Patients who have been diagnosed with irritable bowel syndrome, ulcerative colitis, and Crohn disease. 7)Patients, who are judged to be not appropriate for entry by the trial responsible (collaborative) doctor

Design outcomes

Primary

MeasureTime frame
sensitivity, specificity

Secondary

MeasureTime frame
positive predictive value and negative predictive value of stool occult blood test. positive predictive value and negative predictive value of blood mRNA test.

Countries

Japan

Contacts

Public ContactYoshio Sakai

Kanazawa University school of medicine

yoshios@m-kanazawa.jp076-265-2235

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026