A Cohort Study on Screening and Follow-up of High-risk Population of PDAC Based on EUS

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorPeking Union Medical College Hospital

About this trial

Study objective: The purpose of this study is to establish a prospective follow-up cohort of high-risk groups of pancreatic cancer, screen early pancreatic cancer through EUS and other means according to the existing clinical process, and evaluate each risk factors. And to prospectively collect biological samples to find molecular markers for early diagnosis of pancreatic cancer.

Study design: This is a real world, multicenter, prospective, observational cohort study.

Eligibility criteria

Qualifiers

From the beginning of the study to the end of the study, the 18-80 year old patients who were admitted to Peking Union Medical College Hospital and related research centers and who met the high-risk population of pancreatic cancer understood and were willing to participate in the study and signed the informed consent form.

A. Patients with previous history of pancreatitis (acute or chronic).

B. Patients with pancreatic cancer related genetic background, including immediate relatives with a family history of pancreatic cancer. Or genetic syndrome related to pancreatic cancer. [including hereditary breast cancer ovarian cancer syndrome (HBOCS), carney complex (CNC), familial adenomatous polyps (FAP), hereditary diffuse gastric cancer syndrome (HDGC), juvenile polyposis (JPS), cutaneous malignant melanoma (CMM), hereditary papillary renal cell carcinoma (HPRCC) and Lynch syndrome]

C. Patients with continuous or progressive increase of CA19-9 and CEA.

Disqualifiers

A. Those who are not suitable for endoscopic examination, including but not limited to: poor general condition, serious heart and lung disease, and difficult to tolerate the examination; coagulation disorders; platelets <50 × 10^9/L;those who are not suitable for endoscopic examination after interview by an endoscopic physician.

B. The patient or family member could not understand the conditions and objectives of this study.

Trial design

Treatments tested in this trial

  • Endoscopic ultrasound
  • EUS-Fine needle aspiration

Treatment groups

900 Participants
are divided into 3 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Peking Union Medical College Hospital

Lead sponsor

Beijing Hospital

Collaborator

Tongji Hospital

Collaborator

The First Affiliated Hospital of Xiamen University

Collaborator