The Application of Probe Confocal Laser Endomicroscopy in Pancreatic Tumor Surgery
NCT ID: NCT06289803
Last Updated: 2024-03-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
200 participants
INTERVENTIONAL
2023-09-01
2025-06-30
Brief Summary
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Methods:
Patients who are diagnosed with pancreatic tumor based on preoperative radiographic findings and will undergo radical resection are included in this clinical study. PCLE will be used in surgery to identify tumor is malignant or not, and surgeons will decide procedures of surgery based on outcomes of PCLE. In this present study, clinical trials will be divided into two phases. In the first phase, based on the definitive postoperative pathologic diagnosis, characteristic imaging structures that were collected by PCLE will be identified and primary diagnostic imaging criteria for pancreatic cancer would be developed. In the second phase, this criterion will be used for rapid intraoperative diagnosis of pancreatic cancer and predicting status of resection margin. In addition, accuracy of PCLE will be verified based on postoperative pathologic reports.
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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patients who accept the scan of pCLE
probe confocal laser endomicroscopy
probe confocal laser endomicroscopy will be used to identify the tumor behavior
Interventions
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probe confocal laser endomicroscopy
probe confocal laser endomicroscopy will be used to identify the tumor behavior
Eligibility Criteria
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Inclusion Criteria
2. Patients who have no serious abnormalities of blood system, heart and lung function and immune deficiency and can tolerate surgery.
3. Patients who are not allergic to fluorescein sodium will be included.
Exclusion Criteria
2. Central nervous system disease, mental disease, unstable angina pectoris, congestive heart failure, serious arrhythmia and other uncontrollable serious diseases, unable to tolerate surgery.
3. Patients who have had definitive pathologic diagnosis before surgery will be excluded.
4. Any condition that may impair the safety of patients or the integrity of research data, including serious medical risk factors, medical conditions, and laboratory abnormalities.
18 Years
90 Years
ALL
No
Sponsors
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Fudan University
OTHER
Responsible Party
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Zhijun Bao
Director
Locations
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Huadong Hospital affiliated to Fudan University
Shanghai, Shanghai Municipality, China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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Huadong Hospital of FudanU
Identifier Type: -
Identifier Source: org_study_id
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