Accuracy of Dilution of EUS-FNA Pancreatic Cyst Fluid for Carcinoembryonic Antigen (CEA) Measurement
NCT ID: NCT01494077
Last Updated: 2014-12-12
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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COMPLETED
32 participants
OBSERVATIONAL
2011-04-30
2012-07-31
Brief Summary
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Detailed Description
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A micropipette will be used to ensure exact volumes are measured. The first 1 mL of cystic fluid will be sent to the lab for regular CEA analysis, per standard protocol. The remaining fluid, which would usually be discarded, will then be used for the study. The micropipette will be used to mix 0.75 mL of cyst fluid with 0.25 mL of normal saline (designated sample #2). Next, 0.5 mL of cyst fluid will be mixed with 0.5 mL of normal saline for the next study sample (designated sample #3). These two study samples will be sent to the lab separately using de-identified information, and these values will not be part of the patient's medical record and will not affect clinical management or decision-making. The study samples will be given a unique identifier that will not have any patient identification. The unique identifier will allow the study researchers to link the values to the correct patient by using a password protected program that cannot be accessed by the public.
This study will not require any additional patient participation, and will not impact the length of the procedure. The only additional time will be from the study researchers and the EUS technologists diluting the samples, which will not affect the procedure time itself. If a single patient has more than one cyst, each cyst can be included in the study separately. No additional photographs, videos or data other than the standard data for the procedure will be produced.
Conditions
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Keywords
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Study Design
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PROSPECTIVE
Study Groups
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EUS-FNA of Pancreatic Cyst
Patients who have a pancreatic cyst requiring standard of care EUS-FNA that yields 2.25 ML (or greater) of fluid will be included in the study.
Laboratory processing for results
There is no intervention. Extra fluid that is normally discarded will be processed.
Interventions
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Laboratory processing for results
There is no intervention. Extra fluid that is normally discarded will be processed.
Eligibility Criteria
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Inclusion Criteria
* Cyst must yield 2.25ml (or greater) of fluid
Exclusion Criteria
18 Years
ALL
No
Sponsors
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University of California, Irvine
OTHER
Responsible Party
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Kenneth J. Chang
Professor of Clinical Medicine
Principal Investigators
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Kenneth J. Chang, MD
Role: PRINCIPAL_INVESTIGATOR
University of California, Irvine
Locations
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H. H. Chao Comprehensive Digestive Disease Center
Orange, California, United States
Countries
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Other Identifiers
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HS#2011-8161
Identifier Type: -
Identifier Source: org_study_id