Autoimmune pancreatitis
MONDO:0015175Autoimmune pancreatitis (AIP) is a rare pancreatic disease characterized by chronic non-alcoholic pancreatitis that presents with abdominal pain, steatorrhea, obstructive jaundice and responds well to steroid therapy and is seen in two subforms: type 1 AIP which affects elderly males, involves other organs and has increased immunoglobin G4 (IgG4) levels and type 2 AIP which affects both sexes equally but presents at a younger age and has no other organ involvement or increased IgG4 levels.
Also known as: AIP, lymphoplasmocytic sclerosing pancreatitis
38 clinical trials for this condition and its sub-types, 3 tagged with Autoimmune pancreatitis itself.
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Sub-types of Autoimmune pancreatitis
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Autoimmune pancreatitis type 1 0 trials
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Autoimmune pancreatitis type 2 0 trials
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New diagnostic tool aims to end pancreatitis misdiagnosis
Diagnosis Recruiting nowThis study is testing a new scoring system called OC26 to help doctors more accurately diagnose autoimmune pancreatitis, a condition where the immune system attacks the pancreas. Researchers will review medical data from 82 adults suspected of having the disease. If the OC26 crit…
Sponsor: Military Medical Clinical Center of the Southern Region, Ukraine • Aim: Diagnosis
Last updated Jun 27, 2026 12:39 UTC
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Can a vast image library unlock better pancreatic diagnoses?
Knowledge-focused Recruiting nowResearchers at IRCCS San Raffaele are creating a registry of images and videos from endoscopic ultrasound procedures performed to investigate pancreatic diseases. The study will gather data from about 12,000 patients with conditions like pancreatitis, pancreatic cancer, and neuro…
Sponsor: IRCCS San Raffaele • Aim: Knowledge-focused
Last updated Sep 10, 2026 00:00 UTC