Chronic Pancreatitis Clinical Trial
Official title:
Validation of Endoscopic Ultrasound Criteria for Diagnosis of Chronic Pancreatitis Using Dual Secretin and Cholecystokinin Pancreatic Function Testing as Reference Standard
This is a investigator-initiated, single-center, prospective study to evaluate endoscopic
ultrasound (EUS) as a diagnostic test for chronic pancreatitis (CP). EUS detects
abnormalities of the pancreas that may represent scarring from CP. The validation of any new
test requires a comparison with the best available reference standards. There is no true
"gold standard" for diagnosis of CP; however, pancreatic function testing (PFT) is highly
sensitive for exocrine dysfunction as a surrogate for early fibrosis, and is widely
considered the non-histologic gold standard. There are no well-designed prospective studies
comparing EUS with PFT as reference standard.
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.
n/a
Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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