An Artificial Intelligence System for Multimodal, Multi-class Diagnosis of Pancreatic Cystic Lesions Based on Endoscopic Ultrasonography
Recruiting
Observational Study
Pancreatic Cystic Lesion (PCL)
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
176 (estimated)
Sponsor
Qilu Hospital of Shandong University · Other
Who this trial is looking for
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The aim of this study is to develop and validate an artificial intelligence system named iEUS-PCL (intelligent endoscopic ultrasound system-pancreatic cystic lesions) for detecting and multimodal, multi-class diagnosing pancreatic cystic lesions (PCL) during endoscopic ultrasound (EUS) examination.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. Patients aged ≥18 years scheduled for EUS with suspected pancreatic cystic lesions based on clinical symptoms, medical history, laboratory tests or radiological examinations, and who agree to participate in the research and voluntarily sign the informed consent.
2. Patients w…
Inclusion Criteria:
1. Patients aged ≥18 years scheduled for EUS with suspected pancreatic cystic lesions based on clinical symptoms, medical history, laboratory tests or radiological examinations, and who agree to participate in the research and voluntarily sign the informed consent.
2. Patients with no prior history of treatment for pancreatic lesions.
Exclusion Criteria:
1. Patients with absolute contraindications to EUS examination.
2. Pregnancy or lactating.
3. Uncorrectable coagulopathy (PTT\>50 seconds or INR\>1.5) and/or uncorrectable thrombocytopenia(platelet count\<50×109/L).
4. Upper gastrointestinal obstruction.
5. Patients who underwent surgical treatment or anatomical alterations of the pancreas due to lesions in other thoracic and/or abdominal organs, as well as patients with congenital anatomical abnormalities.
6. Patients who have undergone biliary/pancreatic duct stent placement.
7. Patients who refuse to sign the informed consent.
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