Endoscopic Ultrasound Compared With Pancreatic Function Testing for Diagnosis of Chronic Pancreatitis
NCT ID: NCT00651053
Last Updated: 2016-02-03
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
NA
70 participants
INTERVENTIONAL
2005-05-31
2007-12-31
Brief Summary
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EUS detects parenchymal and ductal features of CP said to correlate with fibrosis. We hypothesize that a predominance of parenchymal fibrosis results in diminished acinar-cell secretion of enzymes. Conversely, a predominance of ductal fibrosis results in impairment of ductal secretion of bicarbonate. Because secretin and cholecystokinin (CCK) PFTs measure unique aspects of pancreatic function (duct-cell and acinar-cell function, respectively), the use of both hormonal stimulants will allow the most comprehensive investigation of the significance of EUS features. There are no studies comparing EUS with combined or dual performance of secretin and CCK PFTs.
The primary objective of this study is to determine the test characteristics of EUS for diagnosis of CP compared with dual secretin- and CCK- stimulated PFTs as reference standard. Secondary objectives include to: 1. Determine the optimal number and relative functional importance of specific EUS criteria, 2. Compare the test characteristics of linear- and radial-array EUS.
190 patients evaluated for pancreatitis or pancreatic-type abdominal pain will undergo the "new test" (radial and linear EUS) and the reference standard (CCK and secretin PFTs). The EUS examinations will be videotaped and interpreted in a blinded fashion. EUS scores will be compared with PFT results to allow the calculation of sensitivity and specificity of linear and radial EUS. Receiver operating characteristics (ROC) analysis will be used to determine the optimal number of EUS criteria for diagnosis.
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Detailed Description
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Conditions
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Study Design
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CROSSOVER
DIAGNOSTIC
NONE
Interventions
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EUS
Sensitivity and specificity of EUS will be compared with PFT as reference standard.
Eligibility Criteria
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Inclusion Criteria
2. Capable of informed consent.
3. If female and not more than 1 year post-menopausal, or surgically sterile, must use medically accepted form of contraception or abstain from sexual activities during study.
4. EUS and CCK ePFT planned for a structural evaluation of the pancreas in patients with pancreatitis or pancreatic-type abdominal pain.
Exclusion Criteria
2. Severe pulmonary disease (Severe asthma, COPD or interstitial lung disease requiring nebulizer treatment or home oxygen, pulmonary hypertension).
3. Severe renal disease (history of chronic renal insufficiency \[creatinine \>2.0\] or chronic hemodialysis).
4. Inability to undergo conscious sedation or general anesthesia.
5. Ongoing illicit drug use or abuse. Must be drug free for \>1 year.
6. Acute pancreatitis within the past 2 months.
7. Prior pancreatic surgery.
18 Years
ALL
No
Sponsors
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ChiRhoClin, Inc.
INDUSTRY
The National Pancreas Foundation
OTHER
The Cleveland Clinic
OTHER
Responsible Party
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Cleveland Clinic Foundatino
Locations
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Cleveland Clinic Foundation
Cleveland, Ohio, United States
Countries
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Other Identifiers
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CRC 2005-01
Identifier Type: -
Identifier Source: org_study_id
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