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Biomarkers of Pancreatic Cancer and New Way to Detection

Identification of AREG for the Detection of Pancreatic Cancer By Biosensor

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04549064
Enrollment
600
Registered
2020-09-16
Start date
2020-09-01
Completion date
2021-12-30
Last updated
2021-08-23

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

Conditions

Pancreatic Cancer

Brief summary

Amphoteric regulatory protein (AREG), a member of epidermal growth factor (EGF) family, is expressed in many tumors.Our study confirmed that the expression of AREG in the serum of patients with pancreatic cancer is significantly higher than that of patients with benign pancreatic diseases and healthy people, which is expected to become a new early serum marker of pancreatic cancer. The serum concentration of AREG was detected by traditional ELISA and compared with CA-199, which was a conventional tumor marker of pancreatic cancer. Next, we compare the advantages of using sensor to detect AREG compared with ELISA.

Detailed description

Serum was collected : pancreatic cancer : healthy control =200:200 Clinical data were collected: age, gender, diagnosis, cancer stage, CA199 level at initial diagnosis, histopathological type, etc. The informed consent of the subjects was obtained before the study, and all experimental procedures were approved by ethics. Draw a summary table of patient characteristics. The level of AREG was detected by ELISA kit and compared with CA199. Fabrication of a new electrochemical biosensor. Characterization of sensor performance.

Interventions

DIAGNOSTIC_TESTdiagnosis of pancreatic cancer

Diagnosis of pancreatic cancer based on the concentration of serum biomarkers

Sponsors

West China Hospital
CollaboratorOTHER
Xi'an Jiaotong University
CollaboratorOTHER
First Affiliated Hospital Xi'an Jiaotong University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
20 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

* The healthy control group had no history of benign pancreatic diseases and other benign and malignant tumors. * Patients with pancreatic cancer did not receive any anti-cancer treatment and had no history of other malignant tumors.The diagnosis of pancreatic cancer patients is based on the final pathological diagnosis; the cancer staging is based on AJCC staging manual.

Exclusion criteria

* Uncontrolled active infection. * Acute or chronic pancreatitis. * It is accompanied by other uncontrolled malignant tumors. * Any other uncontrolled active disease that prevents participation in the trial. * Having a history of mental illness that is difficult to control. * In the opinion of the investigator, the presence of medical or psychiatric history or laboratory abnormalities may increase the risk associated with participation in the study or the administration of the study drug, or may interfere with the interpretation of the results.

Design outcomes

Primary

MeasureTime frameDescription
Diagnosis of Pancreatic Cancerthrough study completion, an average of 1 yearDiagnosis based on the concentration of serum biomarkers

Countries

China

Contacts

Primary Contactwang qi, master
wangqill1024@163.com0086-15991439170

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026