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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000020758
Enrollment
150
Registered
2016-02-01
Start date
2016-06-23
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

pancreatic cancer

Interventions

None listed

Sponsors

Kanazawa University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who meet all of the following criteria below when they are registered. Gender, admission or outpatient clinic will not be assessed. 1. pancreas cancer patient, chronic pancreatitis patient, intraductal papillary mucinous neoplasm, healthy individual. <in case of pancreatic cancer patients> patients who are diagnosed to be pancreatic cancer by image or pathology. <in case of chronic pancreatitis, intraductal papillary mucinous neoplasm> patients who are diagnosed with chronic pancreatitis or intraductal papillary mucinous neoplasm by image or pathology. <in case of healthy individual> the individual who comes to undergo medical check-up and is considered to be healthy judged from the history by the previous year and diagnostic questionnaire on the day of medical check-up. 2. Patients aged more than equal 40 years and less than 90 years old. 3. Patients who give the informed consent.

Exclusion criteria

Exclusion criteria: The patients who meet any of the criteria below will be excluded when they are registered. 1. Patients who have been diagnosed with malignancy(excluding pancreatic cancer) within 5 years of the date of the informed consent. 2. Patients who have been or is currently treated with immunosuppressant, oral steroid within one year of the date of the informed consent. 3. Patients who have been treated with anti-cancer drug within 6 months of the date of the informed consent. 4. Patients who are infected with hepatitis B, hepatitis C or other infectious diseases. 5. 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
1. positive predictive value and negative predictive value of blood mRNA test 2. sensitivity, specificity, positive predictive value and negative predictive value of CEA 3. sensitivity, specificity, positive predictive value and negative predictive value of CA19-9

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