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NCT Number: NCT07030348

Early Diagnosis of Pancreatic Cancer Duodenal Fluid-Based Biomarker Exploratory Study

Purpose Pancreatic cancer is the fourth leading cancer-related mortality disease in the United States, with a five-year survival rate of 11%, and only 10 15% of all pancreatic cancer patients are operable or borderline operable.

Therefore, there is an unmet need for early diagnosis of pancreatic cancer; however, biomarkers related to this are not well understood. This study aims to identify biomarkers for the early diagnosis of pancreatic cancer through duodenal pancreatic juice, which can be easily obtained through an endoscopy.

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Key information

Age range

19 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Asan Medical Center, Seoul, South Korea

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About this study

Pancreatic cancer is the fourth leading cancer-related mortality disease in the United States, with a five-year survival rate of 11%, which is a very poor prognosis, and only 10-15% of all pancreatic cancer patients are operable or borderline operable.

Therefore, there is an unmet need for early diagnosis of pancreatic cancer; however, the biomarkers of humoral fluids associated with the early diagnosis of pancreatic cancer are not well understood.

Duodenal pancreatic fluids can be easily obtained through an endoscopy and contain a large amount of pancreatic fluid secreted by the pancreas, which is known to be a candidate of biomarkers for early diagnosis of pancreatic cancer.

However, there have been few studies using duodenal fluids in Korea. This study aims to prospectively analyze biomarkers for early diagnosis of pancreatic cancer using duodenal fluids obtained by endoscopy in pancreatic and non-pancreatic cancer groups.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Among the patients requiring gastro-duodenal endoscopy, endoscopic ultrasound, or ERCP for medical purposes, the pancreatic cancer group should meet the criteria numbered 1, 2, and either 3 or 4.

  • Be at least 19 years old.
  • Have completed the informed consent for planned upper endoscopy, endoscopic ultrasound, or endoscopic retrograde cholangiopancreatography before the duodenal fluid collection.
  • A biopsy with proven stage I-IV pancreatic ductal adenocarcinoma (PDAC).
  • Suspected pancreatic cancer on imaging and scheduled for an endoscopic ultrasound-guided pancreatic biopsy.

The non-pancreatic cancer group should meet the criteria numbered 1, 2, and either 3 or 4.

  • Be at least 19 years old.
  • Have completed the informed consent for planned upper endoscopy, endoscopic ultrasound, or endoscopic retrograde cholangiopancreatography before the duodenal fluid collection.
  • Patients with pancreatic cystic tumors or patients with acute or chronic pancreatitis.
  • No evidence of a pancreatic disease.

Exclusion criteria

The exclusion criteria for the pancreatic cancer and the non-pancreatic cancer groups will be:

  • Innate or post-surgical anatomy that precludes direct sampling of duodenal fluid.
  • Hemodynamically unstable and unable to have an endoscopy performed.
  • A large amount of ascites fluid that is not controlled and unable to have an endoscopy performed.
  • A coagulation disorder that cannot be corrected and unable to have an endoscopy performed.

Treatment and study plan

Primary outcomes

  1. Identification of Biomarkers for Early Pancreatic Cancer Detection

    Time frame: Up to 1 year from baseline

    Area Under the Receiver Operating Characteristic Curve (AUC) and 95% Confidence Interval (CI) of candidate biomarkers in the training cohort. If the AUC falls within ±5% of the target value (0.94), the optimal cutoff value for pancreatic cancer differentiation will be reported using Youden's Index.

Secondary outcomes

  1. External Validation Using U.S. Samples

    Time frame: Up to 2 year from baseline

    Area under the ROC curve (AUC) of candidate biomarkers in the U.S. validation cohort using cut-off values derived from the Korean training cohort

Other outcomes

  1. Optimizing Sample Collection Volume

    Time frame: Up to 6 month from baseline

    Correlation between duodenal fluid sample volume (mL) and biomarker detection sensitivity (AUC or concentration)

  2. Assessing Racial Differences in Biomarker Expression

    Time frame: Up to 2 year from baseline

    Mean biomarker expression levels in Korean vs. U.S. cohorts as measured in duodenal fluid samples

  3. Evaluating the Impact of Secretin Administration

    Time frame: Up to 1 year from baseline

    Comparison of biomarker concentrations in duodenal fluid with vs. without secretin stimulation

  4. Longitudinal Analysis of non-pancreatic cancer group Samples (Asan Medical Center Only)

    Time frame: Up to 2 year from baseline

    Change in biomarker levels between first and second duodenal fluid samples in non-pancreatic cancer participants

Study contacts

Contact information is provided by the study sponsor or research team.

HyeJin Song, CRC

CONTACT

[email protected]

+82-2-2045-3825

Sponsors and collaborators

Lead sponsor

Do Hyun Park

Other

Collaborators

  • The Cleveland Clinic
  • University of Colorado, Denver

Registry information

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Jun 22, 2025
Registry last updated
Jun 22, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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