Actively Recruiting

Age: 18Years - 80Years
All Genders
NCT06849063

Assessment of the Prognosis of Pancreatic Cancer Patients Using 3D MRE

Led by Yu Shi · Updated on 2026-02-17

200

Participants Needed

1

Research Sites

320 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Pancreatic ductal adenocarcinoma (PDAC), representing 85-95% of pancreatic cancers, is a highly lethal malignancy with a dismal 5-year survival rate below 8%. Emerging evidence highlights the critical need for non-invasive imaging biomarkers to stratify prognosis and guide therapeutic strategies. Notably, the biomechanical properties of PDAC-associated extracellular matrix (ECM), characterized by extensive interstitial fibrosis, are intrinsically linked to tumorigenesis, progression, and metastatic dissemination. Three-dimensional magnetic resonance elastography (3D-MRE), as an advanced imaging modality, enables precise quantification of tissue shear stiffness in both normal pancreatic parenchyma and neoplastic lesions. Significantly, the biomechanical heterogeneity captured by MRE holds untapped potential to serve as a prognostic biomarker for PDAC. Despite its technical merits, no studies to date have systematically explored MRE-derived imaging signatures in predicting PDAC survival outcomes or therapeutic responses, underscoring a pivotal gap in translational oncology research.

CONDITIONS

Official Title

Assessment of the Prognosis of Pancreatic Cancer Patients Using 3D MRE

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Written informed consent is provided
  • Age 18 years or older
  • No history of cancer outside the pancreas
  • No preoperative biliary drainage
  • Confirmed pancreatic ductal adenocarcinoma by tissue biopsy
  • Expected survival of at least three months after surgery or six months of follow-up
Not Eligible

You will not qualify if you...

  • Inability to re-review tissue specimens
  • Poor quality MRE data due to invalid wave data, inconsistent breath holding, intolerable pain, or equipment issues
  • Tumor diameter less than 1.0 cm
  • Withdrawal or dropout during follow-up

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Shengjing hospital of China medical university

Shenyang, Liaoning, China, 110004

Actively Recruiting

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Research Team

Y

Yu Shi, MD.PhD.

CONTACT

Y

Yang Hong, MD.PhD.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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