Plasma cfDNA Fragmentomics for Early pNET Detection and Differential Diagnosis of Solid Pancreatic Tumors
Recruiting now
Conditions studied: Pancreatic Neuroendocrine Tumor, Solid Pancreatic Neoplasms
In brief
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.
Key facts
- Study ID
- NCT05847855
- Run by
- Fudan University
- People needed
- 1000
- Starts
- 2023-02-27
- Expected to finish
- 2026-06-30
- Last updated by the study team
- 2026-03-25
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Age 18 and above, regardless of gender;
- Histopathological diagnosis with non-functional pancreatic neuroendocrine tumor, pancreatic ductal adenocarcinoma or solid pseudopapillary tumor;
- Not receiving any anti-tumor treatment before surgery, including chemotherapy, embolization, ablation, radiotherapy, and molecular targeted therapy;
- No obvious surgical contraindications;
- Able to comply with research plans, follow-up plans, and other protocol requirements;
- Voluntary participation and signed informed consent.
You may not qualify if…
- Pathological diagnosis was not pancreatic neuroendocrine tumor, pancreatic ductal adenocarcinoma or solid pseudopapillary tumor;
- Currently diagnosed with other types of tumors or any cancer history;
- Diagnosed with familial syndromes;
- Receiving anti-tumor treatment before surgery, including chemotherapy, embolization, ablation, radiotherapy, and molecular targeted therapy;
- Ongoing fever or recipient of anti-inflammation therapy within 14 days prior to study blood draw;
- Recipient of blood transfusion within 30 days prior to study blood draw;
- Recipient of organ transplant or prior non-autologous (allogeneic) bone marrow or stem cell transplant;
- Poor health condition and not suitable for blood draw;
- Any other disease/condition deemed not suitable for study enrollment by researcher.
Where it is running
- Fudan University shanghai cancer center — Shanghai, Shanghai Municipality, China (enrolling)
- West China Hospital, Sichuan University — Chengdu, Sichuan, China (enrolling)
Full record on ClinicalTrials.gov
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