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Multicenter study on the clinical usefulness of a new method diagnosing earlier development of pancreatic fibrosis, which targets proteolytic TGF-B-activation reaction.

Not Applicable
Recruiting
Conditions
Chronic pancreatitis
Registration Number
JPRN-UMIN000007271
Lead Sponsor
Department of Gastroenterology and Hepatology, Nagoya University Graduate School of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
100
Inclusion Criteria

Not provided

Exclusion Criteria

1.Patients with infections, difficult to control, for examples active tuberculosis. 2.Patients with severe drug allergy. 3.Patients with difficulty in the performance of endoscopy. 4.Patients with malignancy. 5.Patients with history of anticancer drug. 6.Patients with possible causes developing hepatic fibrosis without alcohol consumption, such as, viral hepatitis, autoimmune hepatitis,non-alcoholic steatohepatitis, and CBD stones etc. 7.Patients with two times or more of the level of normal alanine transaminase (ALT). 8.Patients with interstitial pneumoniae and lung fibrosis. 9.Patients with severe complications. 10.Patients with pregnancy, lactating, possibility of pregnancy, or will of pregnancy. 11.Patients with severe mental disorder.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To study whether the level of TGF-B LAP-D correlates with the stage of chronic pancreatitis.
Secondary Outcome Measures
NameTimeMethod
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