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Biliary Atresia clinical trials

View clinical trials related to Biliary Atresia.

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NCT ID: NCT03273049 Recruiting - Biliary Atresia Clinical Trials

Mapping Disease Pathways for Biliary Atresia

BA
Start date: July 21, 2016
Phase:
Study type: Observational

This project will primarily evaluate the developmental/genetic basis of biliary atresia, the most common cause of liver failure at birth, and which accounts of half of all liver transplants performed worldwide in children.

NCT ID: NCT02922751 Active, not recruiting - Portal Hypertension Clinical Trials

FibroScan™ in Pediatric Cholestatic Liver Disease (FORCE)

FORCE
Start date: November 16, 2016
Phase:
Study type: Observational

Noninvasive monitoring of liver fibrosis is an unmet need within the clinical management of pediatric chronic liver disease. While liver biopsy is often used in the initial diagnostic evaluation, subsequent biopsies are rarely performed because of inherent invasiveness and risks. This study will evaluate the role of non-invasive FibroScan™ technology to detect and quantify liver fibrosis.

NCT ID: NCT02848573 Completed - Clinical trials for to Find Out Non-invasive Indices to Predict the Status of Hepatic Fibrosis in BA Patients.

the Correlation Between Non-invasive Indicators in Patients With Biliary Atresia

Start date: April 2008
Phase: N/A
Study type: Observational

we propose this study and try to find out possible clinical applicable non-invasive imaging indices or its combination with the laboratory indices to predict the status of hepatic fibrosis in BA patients.

NCT ID: NCT02652533 Completed - Biliary Atresia Clinical Trials

Ultrasound Shear Wave Elastography Evaluation of Suspected and Known Biliary Atresia

Start date: September 2016
Phase:
Study type: Observational

The investigators plan to investigate the use of US shear wave elastography (SWE), a newly available imaging technology, in children with suspected/known BA.

NCT ID: NCT02503384 Recruiting - Biliary Atresia Clinical Trials

Clinical and Basic Study for Pediatric Liver Transplantation

CBSPLT
Start date: July 2015
Phase: N/A
Study type: Observational

Background: In mainland China, the development of pediatric liver transplantation (LT) has lagged behind that of adult LT during the past two decades, but it has been progressing immensely in recent years. Renji hospital(shanghai) is currently the largest pediatric transplant center in mainland China. Aim and method: This study is performed for establishment of key techniques for pediatric LT in mainland China, including the indications and timing for pediatric LT, the criteria for donor selections, living donor LT planning, prevention and treatment for posttransplant complications, long-term follow-up management et al.

NCT ID: NCT02471209 Completed - Biliary Atresia Clinical Trials

Biliary Atresia, Hepatic Buffer Response and Sevoflurane

Start date: January 2012
Phase: N/A
Study type: Observational

To evaluate the effects of sevoflurane on hepatic blood flow (HBF) and hepatic arterial buffer response (HABR) in infants with obstructive jaundice by Doppler ultrasound.Twenty-five infants with biliary atresia (1-3 months-of-age) scheduled for a Kasai procedure were enrolled. portal vein blood flow (PBF), hepatic arterial blood flow (HABF) and hepatic blood flow (HBF) were measured by Doppler ultrasound before induction, and after inhalation of 2 and 3% sevoflurane.

NCT ID: NCT02298218 Completed - Clinical trials for Biliary Atresia, Kasai Portoenterostomy Status

Clinical Study About the Role of COX-2 Inhibitor in Liver Cirrhosis With Biliary Atresia

Start date: September 2009
Phase: Phase 4
Study type: Interventional

In this clinical study, meloxicam will be used to the patients who are older than 2 years and underwent Kasai portoenterostomy to treat their biliary atresia before. Before and after the medication, their liver stiffness scores will be checked using hepatic Fibroscan. Liver stiffness scores will be compared before and after the medication of meloxicam, and the roll of the COX-2 inhibitor (meloxicam) in the patients with biliary atresia in releasing their hepatic fibrosis. Also, the side effect of the drug will be checked. The intervention drug, meloxicam is safe medicine which is used to treat pain or inflammation caused by osteoarthritis or rheumatoid arthritis in adults and children who are at least 2 years old. It may also be used for purposes not listed in the medication guide. It will be taken once a daily with a dose of 0.125 mg/kg/day (high-dose group) or 0.06 mg/kg/day (low-dose group). After 6 months of medication, the maintenance will be decided by the comparison of liver stiffness score before and after the intervention.

NCT ID: NCT02292862 Completed - Biliary Atresia Clinical Trials

Maternal Microchimerism in Lymph Nodes of Infants With Biliary Atresia at Time of Kasai's Operation

K-LNMC
Start date: November 2012
Phase: N/A
Study type: Observational

Maternal microchimerism has been discussed as an etiological mechanism in infantile (perinatal) biliary atresia (BA). In Kasai's operation (resection of the liver hilum plaque followed by hepato-portoenterostomy) surgeons frequently encounter swollen portal and mesenteric lymph nodes. Lymph nodes were sampled during Kasai' s operation and examined for maternal DNA.

NCT ID: NCT02137668 Recruiting - Clinical trials for Primary Sclerosing Cholangitis

Treating Primary Sclerosing Cholangitis and Biliary Atresia With Vancomycin

Start date: July 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is twofold. First, is to determine whether vancomycin is effective in the early treatment of Biliary Atresia (BA) and Primary Sclerosing Cholangitis (PSC), and if so, by what mechanism. Secondly, to characterize human intestinal microbial communities and their interactions with the host.

NCT ID: NCT01854827 Completed - Biliary Atresia Clinical Trials

Safety Study of Intravenous Immunoglobulin (IVIG) Post-Portoenterostomy in Infants With Biliary Atresia

PRIME
Start date: October 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The Children Liver Disease Research and Education Network (ChiLDREN) is conducting a clinical trial to determine the feasibility, acceptability, tolerability and safety profile of IVIG treatment administered to infants after hepatic portoenterostomy (HPE) for biliary atresia, as well as investigate preliminary evidence of activity and explore mechanisms of action.