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Cholestasis clinical trials

View clinical trials related to Cholestasis.

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NCT ID: NCT01381939 Completed - Clinical trials for Intrahepatic Cholestasis

Induction of Labor in Intrahepatic Cholestasis of Pregnancy

ILICP
Start date: January 2000
Phase: N/A
Study type: Observational

Induction of Labour in Intrahepatic Cholestasis of Pregnancy (ICP) has become a common procedure in management of ICP to avoid fetal complications. Surprisingly, this empirical approach has not been evaluated as to delivery complications and fetal outcome as yet. The investigators now examine weather ICP affects (i) delivery procedures chosen, in particular the incidence of caesarian section, (ii)fetal and maternal outcome in induced labor, and (iii)possible impact of bile acids and UDCA treatment in a retrospective cohort study based on approximately 5000 induced deliveries at Danderyd Hospital, Karolinska Institutet, Stockholm. The investigators analyze data on on previous deliveries, BMI, medical history and medical book data. Primary endpoint is the risk of caesarian section.

NCT ID: NCT01373918 Completed - Cholestasis Clinical Trials

Low Dose Fat for the Prevention of Liver Disease in Babies With Gastrointestinal Disorders

Start date: December 2010
Phase: Phase 4
Study type: Interventional

Neonates with congenital/acquired gastrointestinal disorders are at high risk for Parenteral Nutrition Associated Cholestasis (PNAC). Besides enteral nutrition, standard therapies to prevent and treat PNAC have been limited and marginal. Recently, the dose and composition of standard intravenous fat emulsions have implicated in the development and progression of PNAC. In this study, neonates with congenital/acquired gastrointestinal disorders will be randomized, in a unblinded fashion, to receive either the standard dose of an intravenous omega-6 fatty acid emulsion or a low dose of an intravenous omega-6 fatty acid emulsion throughout their course of PN or until hospital discharge, death or 100 days of life, whichever comes first. The primary outcome will be the presence of cholestasis.

NCT ID: NCT01356030 Completed - Jaundice Clinical Trials

Endoscopic Ultrasound Versus Endoscopic Retrograde Cholangiopancreatography (ERCP) Tissue Sampling for the Diagnosis of Suspected Pancreatico-Biliary Cancer

Start date: May 2011
Phase: N/A
Study type: Interventional

The two most commonly used methods to biopsy suspected pancreaticobiliary masses are (1) endoscopic ultrasound guided fine-needle aspiration (EUS-FNA) and (2) cytology brush biopsies obtained during endoscopic retrograde cholangiopancreatography (ERCP). At most centers, the specific method used depends on the availability of the technology and local expertise. Although it is believed that EUS-FNA is more accurate than ERCP brushings, there have been no head-to-head comparisons. The investigators' hypothesis is that EUS-FNA is superior to ERCP in obtaining tissue biopsies of pancreaticobiliary tumors, and the investigators aim to directly compare the two techniques.

NCT ID: NCT01343160 Completed - Biliary Strictures Clinical Trials

Removable GORE VIABIL® Biliary Endoprosthesis for Treatment of Benign Biliary Strictures

Start date: April 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to generate clinical data to support the use of GORE® VIABIL® Biliary Endoprosthesis in the endoscopic and percutaneous treatment of benign biliary strictures.

NCT ID: NCT01339078 Completed - Clinical trials for Biliary Strictures Post Liver Transplantation

Trial Comparing Kaffes Stent With Plastic Prosthesis in the Treatment of Anastomotic Biliary Strictures Post Orthotopic Liver Transplantation

Start date: September 2011
Phase: N/A
Study type: Interventional

Biliary anastomotic strictures (post liver transplantation) occur in 15-20 % of the cases. Biliary stenting using plastic prosthesis during a period of 1 year is the treatment of choice. Problematic in this approach is the regular change, necessary to overcome occlusion of the stent, resulting in cholestasis and/or infection. This change needs to be performed every 3 months or more frequently in patients with symptoms of stent occlusion. The Kaffes stent (RMS) is a metallic removable stent, especially constructed for the treatment of biliary anastomotic strictures post liver transplantation. The advantage could be that this stent is less prone to occlusion with a lower change frequency (e.g. every 6 months). No randomized, controlled trial (RCT) or data exist comparing plastic stenting versus Kaffes stenting.

NCT ID: NCT01323907 Withdrawn - Clinical trials for Total Parenteral Nutrition-induced Cholestasis

Compassionate Use of Omegaven IV Fat Emulsion

Start date: January 2011
Phase: N/A
Study type: Interventional

The purpose of the study is to provide use of Omegaven in children with life threatening Total Parenteral Nutrition (TPN) associated cholestasis when all other medical and surgical treatments/therapies have been either ineffective or not feasible in the treatment of this serious condition. This is a compassionate use protocol.

NCT ID: NCT01297933 Approved for marketing - Clinical trials for Short Bowel Syndrome

Compassionate Use of Omegaven for Pediatric Patients With Parenteral Nutrition Associated Liver Disease

Omegaven
Start date: n/a
Phase:
Study type: Expanded Access

A compassionate use protocol to provide Omegaven to pediatric patients with parenteral nutrition (PN) dependence and parenteral nutrition associated liver disease (PNALD).

NCT ID: NCT01271179 Completed - Clinical trials for Liver Transplantation

Study of Sequential Perfusion of Liver Grafts to Prevent Nonanastomotic Biliary Strictures After Liver Transplantation

Start date: July 2004
Phase: N/A
Study type: Interventional

The study was designed to investigate whether, compared with conventional sole perfusion with high-viscosity solution of University of Wisconsin (UW), sequential perfusion of liver grafts with low-viscosity and high-viscosity preservation solutions could further decrease the incidence of nonanastomotic biliary strictures (NAS) after liver transplantation.

NCT ID: NCT01252043 Recruiting - Children Clinical Trials

Retrospective Review of CT and MR in Pediatric Patients With Cholestasis

Start date: October 2010
Phase: N/A
Study type: Observational

The investigators will try to predict the risk of esophageal varices (EVs) in long-term BA survivors using noninvasive computed tomography (CT) or magnetic resonance (MR) indices and the measurement of transverse diameters of paraesophageal and gastroesophageal veins.

NCT ID: NCT01247012 Recruiting - Cholestasis Clinical Trials

Minimization of IntraLipid Versus Omegaven

MILOve
Start date: December 2010
Phase: Phase 2/Phase 3
Study type: Interventional

Prolonged use of parenteral nutrition can lead to parenteral nutrition associated liver disease (PNALD). The purpose of this study is to determine the effect of treatment with a smaller amount lipid minimization) of our standard soybean oil based intravenous lipid emulsion (Intralipid) versus a fish-oil based lipid emulsion (Omegaven) in infants with severe cholestasis.