RecruitingNCT05847855

Plasma cfDNA Fragmentomics for Early pNET Detection and Differential Diagnosis of Solid Pancreatic Tumors

A Prospective Study of Plasma Cell-free DNA Fragmentomics for Early Detection of Pancreatic Neuroendocrine Tumors and Differential Diagnosis of Solid Pancreatic Tumors


Sponsor

Fudan University

Enrollment

1,000 participants

Start Date

Feb 27, 2023

Study Type

OBSERVATIONAL

Conditions

Summary

This prospective study aims to evaluate the sensitivity and specificity of an integrated model using fragmentomic profiles of plasma cell-free DNA for early detection of pancreatic neuroendocrine tumors and differential diagnosis of solid pancreatic tumors.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether analyzing DNA fragments floating in the blood (called cell-free DNA or cfDNA) can help detect and distinguish between different types of pancreatic tumors earlier and more accurately — without invasive biopsy. **You may be eligible if...** - You are 18 or older - You have been diagnosed with one of three types of solid pancreatic tumors: a non-functional pancreatic neuroendocrine tumor, pancreatic ductal adenocarcinoma (the most common type of pancreatic cancer), or solid pseudopapillary tumor - You have not received any anti-cancer treatment before your surgery - You are scheduled to have surgery to remove the tumor **You may NOT be eligible if...** - You have received chemotherapy, radiation, or other anti-cancer treatments before surgery - You have another active cancer at the same time - You are unable or unwilling to provide consent or a blood sample Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIAGNOSTIC_TESTBlood collection

Blood collection for fragmentomic profiles of plasma cell-free DNA. The sub-center shall use the same blood collection consumables (EDTA anticoagulant vacutainer tubes) and blood collection volume (10ml) as the main center; plasma separation shall be completed within 2 hours after blood collection, and all operations shall comply with the study's unified SOP.


Locations(2)

Fudan University shanghai cancer center

Shanghai, Shanghai Municipality, China

West China Hospital, Sichuan University

Chengdu, Sichuan, China

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NCT05847855


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