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Cholangitis clinical trials

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NCT ID: NCT03175471 Recruiting - Clinical trials for Primary Sclerosing Cholangitis

MRI Based Biomarkers in Pediatric Autoimmune Liver Disease

Start date: January 17, 2017
Phase:
Study type: Observational

Autoimmune liver diseases (AILD), which include Primary Sclerosing Cholangitis (PSC) and Autoimmune Hepatitis (AIH) are a common etiological factors for chronic liver disease among adolescents. In all these conditions, autoimmune lymphocyte responses are thought to orchestrate inflammatory injury against hepatocytes (primarily in AIH) or cholangiocytes (in PSC). In this proposal we aim to evaluate the Magnetic Resonance Imaging (MRI) modalities; MR cholangiopancreatography (MRCP) and MR elastography (MREL), as non-invasive biomarkers to assess two primary pathophysiological processes of AILD: bile duct damage and liver fibrosis. In this cross-sectional study MRI based findings of bile duct injury and liver fibrosis will be correlated with both liver histology and circulating biomarkers of these disease processes.

NCT ID: NCT03146936 Recruiting - Clinical trials for Cholangitis, Sclerosing

Swiss Primary Sclerosing Cholangitis Cohort Study

Start date: February 28, 2017
Phase:
Study type: Observational [Patient Registry]

Research project in which biological material is sampled and health-related personal data is further used and collected. Coded data are used.

NCT ID: NCT03146910 Recruiting - Clinical trials for Liver Cirrhosis, Biliary

Swiss Primary Biliary Cholangitis Cohort Study

Start date: February 15, 2017
Phase:
Study type: Observational [Patient Registry]

Research project in which biological material is sampled and health-related medical data is collected. In addition, already existing health-related medical data are used for further research. Coded data are used.

NCT ID: NCT03133026 Recruiting - Cholangitis Clinical Trials

Cholangioscopic Assessment of Occluded Biliary Stent and Role of Biliary Radiofrequency Ablation

Start date: June 2016
Phase: N/A
Study type: Interventional

Primary Objective: To document state-of- the-art multi-modality management of occluded biliary SEMS aiming to minimize number of reinterventions while providing symptom relief without procedure-related serious adverse events. NOTE: This study will be hypothesis-generating for an anticipated randomized controlled study (RCT) to compare outcomes of placement of a plastic stent inside the occluded SEMS to outcomes of the proposed multi-modality approach.

NCT ID: NCT03087656 Recruiting - Cholangitis Clinical Trials

Antibiotics to Decrease Post ERCP Cholangitis

Start date: March 29, 2017
Phase: Phase 4
Study type: Interventional

Endoscopic retrograde cholangiopancreatography (ERCP) is an endoscopic procedure used to treat bile duct stones, obstructive jaundice, biliary leaks, and a variety of other conditions. There is active debate whether antibiotics should be given prophylactically for ERCP outside of high risk indications including primary sclerosing cholangitis. In part this is due to a lack of appropriately powered clinical trials with adequate follow up. The aim will be to assess whether prophylactic antibiotics decrease the rate of post ERCP cholangitis as defined by the Revised Tokyo Criterion.

NCT ID: NCT02997878 Recruiting - Clinical trials for Hepatitis, Autoimmune

Selected Mesenchymal Stromal Cells to Reduce Inflammation in Patients With PSC and AIH

Merlin
Start date: December 7, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

MERLIN is an adaptive, single arm, multi-centre, phase IIa multi-disease clinical trial. It is designed to: i) Determine dose safety of ORBCEL-C™ (selected Mesenchymal stromal cells derived from human umbilical cord) ii) Evaluate treatment activity through assessment of biomarkers (for patients treated at the highest safe dose only (HSD)) This trial will determine the Highest Safe Dose (HSD) that can be administered by observing for occurrence of dose limiting toxicity (DLT). Upon completion of this trial we hope to be able to justify and conduct separate, larger scale trials using ORBCEL-C™.

NCT ID: NCT02936596 Recruiting - Cholestasis Clinical Trials

Remission Induction of Primary Biliary Cholangitis-autoimmune Hepatitis Overlap Syndrome

Start date: December 2016
Phase: N/A
Study type: Interventional

Biochemical response of primary biliary cholangitis-autoimmune hepatitis overlap syndrome induced by ursodeoxycholic acid only or combination therapy of immunosuppressive agents

NCT ID: NCT02797665 Recruiting - Clinical trials for Obstructive Jaundice

Treatment of Obstructive Jaundice in Autoimmune Pancreatitis and/or Immunoglobulin G4-related Sclerosing Cholangitis by Corticosteroids

Start date: May 2016
Phase: N/A
Study type: Interventional

This study evaluates corticosteroids in the treatment of obstructive jaundice in autoimmune pancreatitis and/or immunoglobulin G4 (IgG4)-related sclerosing cholangitis in adults. Half of participants will receive corticosteroids alone, while the other half will receive corticosteroids with biliary stent at the beginning.

NCT ID: NCT02701166 Recruiting - Clinical trials for Primary Sclerosing Cholangitis

The Effect of Bezafibrate on Cholestatic Itch

FITCH
Start date: February 2016
Phase: Phase 3
Study type: Interventional

Randomized double blind placebo controlled trial to evaluate the antipruritic effect of bezafibrate in patients with moderate to severe cholestatic itch.

NCT ID: NCT02605213 Recruiting - Clinical trials for Primary Sclerosing Cholangitis

Effect and Safety of Oral Vancomycin in Primary Sclerosing Cholangitis Patients

Start date: September 2015
Phase: Phase 4
Study type: Interventional

Primary sclerotic cholangitis (PSC) is an inflammatory process of sclerotic cholangitis that involves intra and extra hepatic biliary system. There is no curative treatment for this disorder. Supportive and conservative treatments are the most common therapies that used for this disease. Although treatments such as ursodeoxycholic acid (UDCA) are recommended in some situations but whereas a hypothesis is stimulatory effect of intestinal anaerobic bacteria such as cholestridium difficile as pathogenesıs of PSC, so use of antibiotics is recommended for treatment of these patients. Therefore according to the great role of anaerobic bacteria such as cholestridium difficile in pathogenesis, antibiotics such as metronidazole and vancomycin can be counted as recommended therapies in PSC. In addition some studies correlated this effect of vancomycin to its immunomudulatory effect the cause reduction of inflammation in biliary system. But with all this detail there is no finality about effectiveness of antibiotic therapy and accordingly in this study the investigators compare oral vancomycin effect versus placebo in primary sclerosing cholangitis patients. In this double blind clinical trial 30 primary sclerosing cholangitis patients that divided in two 15 persosns group with Block Randomization method. in this study one group receive 250 mg oral vancomycin every 6 hours and other group receive placebo. The study duration is 12 weeks . The baseline laboratory tests and 1 month and 3 months after treatment concept of; Alkaline phosphatase, ALT, AST, GGT and serum total bilirubin and clinical manifestations such as tiredness, itching and probable adverse effects such as hypotension accompanied by flushing,erythematous rash on face and upper body (red neck or red man syndrome), chills and drug fever, eosinophilia and reversible neutropenia.