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A prospective cohort study of EUS-FNA combined with improved ROSE method for improving the diagnostic rate of pancreatic solid lesion puncture

A prospective cohort study of EUS-FNA combined with improved ROSE method for improving the diagnostic rate of pancreatic solid lesion puncture

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500110316
Enrollment
Unknown
Registered
2025-10-11
Start date
2025-11-01
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Pancreatic cancer

Interventions

Gold Standard:Collect the pathological diagnosis results and treatment information of the two groups (if surgery is performed, collect postoperative pathology
if chemotherapy is administered, collect imaging data during chemotherapy
if under follow-up observation, collect imaging data). Use the final surgical pathology or imaging results at 6 months of follow-up.
Index test:EUS-FNA diagnosis combined with modified ROSE

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients suspected of having a solid pancreatic lesion based on imaging (CT or MRI), aged 18-80 years, with no obvious contraindications to puncture (such as coagulation disorders or gastrointestinal obstruction); 2. Planned to undergo EUS-FNA examination before surgery or chemotherapy to obtain histopathological or cytopathological diagnosis; 3. The subject personally agrees and voluntarily signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Have clear puncture contraindications (coagulation dysfunction, gastrointestinal obstruction, etc.); 2. Those who refuse to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
Diagnosis rates in both groups;

Secondary

MeasureTime frame
specificity;The accuracy of the two groups of diagnoses;number of punctures;Negative predicted value;Post-puncture complications;operating time;sensitivity;Positive predicted value;

Countries

China

Contacts

Public ContactCai Yunlong

Peking University First Hospital

cyl030104@163.com+86 10 8357 2437

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026