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Cholangitis clinical trials

View clinical trials related to Cholangitis.

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NCT ID: NCT02917408 Completed - Liver Cirrhosis Clinical Trials

Retrospective Study About Primary Biliary Cholangitis During January 2001 to July 2016 at West China Hospital

Start date: September 2016
Phase:
Study type: Observational

Retrospective study of all patients diagnosed with primary biliary cholangitis during January 2001 to July 2016 at West China Hospital by review of medical records. The following variables will be retrospectively studied: age, sex, first symptoms, clinical characteristics, pathology, treatment, stage, complications of cirrhosis, other autoimmune diseases and long-term outcome.

NCT ID: NCT02884557 Completed - Clinical trials for Inflammatory Bowel Diseases

NKT Role in the Regulation of the Inflammatory Bowel Disease

NKT-CSP/MICI
Start date: May 2013
Phase: N/A
Study type: Interventional

Inflammatory bowel diseases (IBD) include Crohn's disease (CD) and ulcerative colitis (UC). These diseases are a public health problem because they concern many patients (1 case in 1000). IBDs are characterized by dysregulated immune response against luminal antigens causing chronic inflammation of the gut in genetically predisposed individuals. Their exact cause is unknown and there is currently no cure. The primary sclerosing cholangitis (PSC) is a liver inflammatory disease of unknown origin that is known to be strongly associated with IBD. An important clinical observation highlights the mild symptoms of IBD when associated to the PSC. Conversely, treating PSC by liver transplant or immunosuppressive drugs is associated with a progression of intestinal inflammation. Based, on these clinical findings that suggest a protective effect regulator of liver inflammation on intestinal inflammation, and on the results obtained by our group in mouse models that identified the natural killer T cell (NKT) as essential in control of experimental colitis, the project aims to determine, using PCR, if the expression of NKT cell markers are increased in the colon of patients with PSC+IBD compared to patients with IBD alone or PSC alone.

NCT ID: NCT02808312 Completed - Clinical trials for Nonalcoholic Steatohepatitis (NASH)

Pharmacokinetics and Pharmacodynamics of Cilofexor in Adults With Normal and Impaired Hepatic Function

Start date: July 13, 2016
Phase: Phase 1
Study type: Interventional

The primary objective of this study is to evaluate the single-dose pharmacokinetics of cilofexor in adults with impaired hepatic function relative to matched, healthy controls with normal hepatic function.

NCT ID: NCT02736708 Completed - Clinical trials for Primary Sclerosing Cholangitis

Registry Trial to Determine pCLE Image Interpretation Criteria and Preliminary Accuracy for PSC Biliary Strictures

PSCRegistry
Start date: January 2013
Phase:
Study type: Observational [Patient Registry]

Primary sclerosing cholangitis (PSC) 1. Prospectively validate interpretation criteria for the characterization of PSC strictures 2. Prospectively evaluate the accuracy of pCLE for the characterization of PSC strictures (differentiation between malignant vs. non malignant strictures), using the newly developed interpretation criteria 3. Evaluate the feasibility and safety of pCLE for the characterization of PSC strictures

NCT ID: NCT02712736 Completed - Clinical trials for Primary Sclerosing Cholangitis

Quality of Life in Patients With Primary Sclerosing Cholangitis

QOL in PSC
Start date: July 1, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the healthcare-related quality of life (HRQOL), the impact of risk of liver transplant and risk of malignancy on HRQOL, and the complementary and alternative medicine use in patients with PSC.

NCT ID: NCT02705638 Completed - Clinical trials for IgG4-related Disease

Treatment of IgG4-Related Disease With Revlimid and Rituximab

TIGR2
Start date: April 2016
Phase: Phase 1
Study type: Interventional

Among persons with Immunoglobulin G subclass 4 Related Disease (IgG4)-related disease who have persistent or recurrent disease despite standard therapies, does combination therapy with rituximab and revlimid cause a sustained disease remission?

NCT ID: NCT02704364 Completed - Clinical trials for Primary Sclerosing Cholangitis

Phase 2 Study of NGM282 in Patients With Primary Sclerosing Cholangitis

Start date: March 2016
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety, tolerability, and activity of NGM282 in patients with Primary Sclerosing Cholangitis.

NCT ID: NCT02659696 Completed - Clinical trials for Primary Biliary Cirrhosis

Nalfurafine Hydrochloride for Pruritus in Patients With Primary Biliary Cholangitis

Start date: September 2015
Phase:
Study type: Observational

Nalfurafine hydrochloride is a selective kappa-opioid receptor agonist developed in Japan, and in May 2015 the use of nalfurafine hydrochloride was officially approved in Japan for pruritus in patients with chronic liver diseases including PBC. In the current study, the investigators aimed to assess pruritus and overall QOL before and after administration of nalfurafine hydrochloride in patients with PBC. Furthermore, the investigators took serum sample from the enrolled patients and examine the association of pruritus with possible biomarkers.

NCT ID: NCT02653625 Completed - Clinical trials for Primary Sclerosing Cholangitis

PERSEUS: Preliminary Efficacy and Safety of Cenicriviroc in Adult Participants With Primary Sclerosing Cholangitis

Start date: March 14, 2016
Phase: Phase 2
Study type: Interventional

This is an open label, proof of concept (PoC) study of Cenicriviroc (CVC) in adult participants with Primary Sclerosing Cholangitis (PSC). The main objective of this PoC study is to assess changes in alkaline phosphatase (ALP) both individually and as a group, over 24 weeks of treatment with CVC.

NCT ID: NCT02647593 Completed - Choledocholithiasis Clinical Trials

The Clinical Characteristics of the Patients With Choledocholithiasis Without Cholangitis

Start date: October 2, 2012
Phase:
Study type: Observational

Laboratory change induced by common bile duct (CBD) stone is in general observed as the higher elevation of alkaline phosphatase (ALP) and gamma-glutamyl transpeptideas (ɤ-GT), in comparison to those of aspartate aminotransferase (AST) and alanine aminotransferase (ALT). However, some patients with CBD stone show the marked increased level of aminotransferase, which sometimes leads to misdiagnose those as liver disease caused by viral hepatitis, ischemia, and drug toxicity. The aim of this study is to investigate the clinicopathologic features of patients with CBD stones with the high level of aminotransferase in serum.