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Clinical research on the early diagnosis of liver, gallbladder and pancreatic malignancies was established based on dendritic cell cluster target (DC-SCT) detection technology

Clinical research on the early diagnosis of liver, gallbladder and pancreatic malignancies was established based on dendritic cell cluster target (DC-SCT) detection technology

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600120818
Enrollment
Unknown
Registered
2026-03-20
Start date
2026-03-20
Completion date
Unknown
Last updated
2026-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Malignant tumors of the liver, gallbladder, and pancreas

Interventions

Gold Standard:Perform a biopsy or surgical procedure for pathological examination and obtain a definitive pathology report
Index test:Liquid Chromatography-Mass Spectrometry (Model: Waters Xevo G2-XS Q-TOF)

Sponsors

The First Affiliated Hospital of Xiamen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients with newly diagnosed liver, gallbladder, or pancreatic masses can undergo puncture or surgery for pathological examination and obtain a definitive pathological diagnosis report; 2. Normal liver, kidney, and bone marrow function: WBC >= 3.5 × 10^9 /L, PLT >= 90 × 10^9 /L, and Hb >= 90 g/L; serum Cr <= 1.5 × ULN (upper limit of normal) and serum BIL <= 1.5 × ULN; ALT, AST <= 2.5 × ULN; 3. Age 18–70 years.

Exclusion criteria

Exclusion criteria: 1.Patients with hepatobiliary and pancreatic space-occupying lesions who are unable to obtain a definitive pathological diagnosis, or patients who cannot obtain a clear pathological diagnosis report. 2.Patients who have received chemotherapy, radiotherapy, immunotherapy, or targeted therapy within the past 3 months; 3.Patients with concomitant other malignancies; 4.Pregnant or lactating women; 5.Patients with coagulopathy (e.g., INR > 1.5) or a tendency to bleed; 6.Patients with severe infection or active autoimmune diseases; 7.Patients who are unable to cooperate with sample collection or follow-up;

Design outcomes

Primary

MeasureTime frame
Positive percent agreement;

Secondary

MeasureTime frame
Negative agreement rate;

Countries

China

Contacts

Public ContactShen Dongyan

The First Affiliated Hospital of Xiamen University

shendongyan@163.com+86 592 2137507

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026