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Cholestasis clinical trials

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NCT ID: NCT05043194 Recruiting - Clinical trials for Cholestasis of Parenteral Nutrition

Ursodeoxycholic Acid Prevents Total Parenteral Nutrition Cholestasis

UDACPPNAC
Start date: January 1, 2021
Phase: N/A
Study type: Interventional

This study aims to confirm whether the preventive use of ursodeoxycholic acid on the 5th day after birth in preterm infants who started parenteral nutrition therapy can reduce the occurrence of enteral nutrition-related cholestasis in preterm infants. This study examined the safety and efficacy of ursodeoxycholic acid (UDCA) in preventing Cholestasis Associated with Total Parenteral Nutrition in preterm infants.

NCT ID: NCT04992585 Completed - Clinical trials for Bile Duct Obstruction

Primary Versus Secondary Metal Stent Implantation in PTBD

Start date: March 1, 2011
Phase: N/A
Study type: Interventional

The aim is to compare percutaneous transhepatic biliary drainage (PTBD) with primary metal stent implantation (one stage-procedure) with PTBD with secondary metal stent implantation in terms of adverse events.

NCT ID: NCT04922580 Completed - Clinical trials for Intrahepatic Cholestasis of Pregnancy

Predictors of Adverse Neonatal Outcomes in Intrahepatic Cholestasis of Pregnancy

Start date: January 1, 2012
Phase:
Study type: Observational

Many studies have attempted to find the predictors of adverse neonatal outcome in women with Intrahepatic Cholestasis of Pregnancy(ICP).Serum total bile acid level exceeding 40 µmol/L has been associated with increased risk of meconium staining, low Apgar scores, preterm delivery, and stillbirth.Other predictors such as level of transaminases, history of cholelithiasis, and hepatitis virus infection have been studied but the results are inconclusive.A more comprehensive investigation involving multiple neonatal outcomes and a wide variety of outcome predictors is needed in order to establish guidelines for optimal timing of delivery in pregnancies complicated by ICP. The aim of our study was to evaluate wide variety of predictors of adverse neonatal outcomes in a large cohort of women with ICP .

NCT ID: NCT04915703 Recruiting - Clinical trials for Bile Duct Obstruction

Flushing of Internalized Percutaneous Transhepatic Biliary Drainage Catheters

FLUSH
Start date: June 1, 2022
Phase: N/A
Study type: Interventional

Percutaneous transhepatic biliary drainage (PTBD) is a drainage method for biliary obstruction. Patients with a PTBD catheter often need multiple re-interventions because of symptoms of catheter obstruction such as pain, jaundice, pruritus, leakage and/or fever. The onset of these symptoms results in hospital visits, opening of the external catheter of an internal external PTBD and re-interventions. The investigators hypothesize that daily flushing of an internal external biliary catheter will increase the time-to-symptom-onset.

NCT ID: NCT04890886 Not yet recruiting - Diabetes Mellitus Clinical Trials

Magnetic Resonance Imaging and Thermal Imaging of Adiposity in Neonates of Women With Metabolic Diseases

MRI-TIME
Start date: June 1, 2021
Phase:
Study type: Observational

There is limited knowledge about the extent of the impact of maternal metabolic diseases (MD) and/or alterations in maternal serum lipid content upon neonatal lipid distribution and phenotypes. This observational feasibility study aims to investigate the effect of maternal MD on fat distribution, lipid content and metabolic phenotype of different neonatal tissues. We will explore whether differences in tissue fat distribution and lipid content are observed in the neonates of women with MD during pregnancy, compared to those who have a healthy, uncomplicated pregnancy and if there are changes in how the different tissues work (e.g. cardiac function). If there is evidence to show that there are alterations during pregnancy in children of women with MD, this will help inform potential interventions to ensure optimal child health.

NCT ID: NCT04807478 Withdrawn - Malnutrition Clinical Trials

Safety of Omegaven in Pediatric Patients With Parenteral Nutrition-Associated Cholestasis (PNAC)

Start date: April 1, 2022
Phase:
Study type: Observational

This study will demonstrate Short-, mid-, and long-term safety in pediatric patients with Parenteral Nutrition-Associated Cholestasis treated with Omegaven®, which is indicated as a source of calories and fatty acids in this patient population

NCT ID: NCT04805450 Recruiting - Clinical trials for Malignant Bile Duct Obstruction

Sems Placement With and Without Biliary Sphincterectomy in Patients With Malignant Biliary Obstruction

SEMS
Start date: October 1, 2015
Phase: N/A
Study type: Interventional

Placement of biliary self expanding metal stent (SEMS) is indicated when malignant common bile duct obstruction is encountered [1]. Currently, there is still controversy regarding the use of endoscopic sphincterotomy (EST) before the placement of biliary stents [2-5]. The aim of this prospective randomized, multicenter study is to investigate the role of EST before fully covered SEMS placement in patients with neoplastic biliary obstruction.

NCT ID: NCT04787419 Active, not recruiting - Clinical trials for Cholestatic Liver Disease

Probiotics in Pediatric Chronic Cholestasis

Start date: September 1, 2020
Phase: Phase 2/Phase 3
Study type: Interventional

double blinded RCT (probiotics vs placebo) given to pediatric patients with chronic cholestasis for 4 weeks duration. baseline characteristics (antropometry, gastrointestinal symptoms, laboratory examinations) would be compared pre vs post treatment

NCT ID: NCT04759794 Recruiting - Clinical trials for Bile Duct Obstruction, Extrahepatic

Clinical Validation of an Immunocytochemistry Method Using MARS1

MARS1
Start date: February 4, 2021
Phase: N/A
Study type: Interventional

The sensitivity of brushing cytology used to distinguish the cause of biliary strictures is low and clinical usefulness is not secured. The aim of this study was to validate the clinical usefulness of a new differential staining method for cytology which is difficult to differentiate by the conventional staining method using biliary cancer-related protein expressed only in bile duct cancer.

NCT ID: NCT04729751 Active, not recruiting - Alagille Syndrome Clinical Trials

A Study to Evaluate the Safety and Tolerability of Maralixibat in Infant Participants With Cholestatic Liver Diseases Including Progressive Familial Intrahepatic Cholestasis (PFIC) and Alagille Syndrome (ALGS).

RISE
Start date: September 9, 2021
Phase: Phase 2
Study type: Interventional

This study is designed to assess whether the investigational drug maralixibat, is safe and well tolerated in children <12 months of age with Alagille Syndrome [ALGS] or Progressive Familial Intrahepatic Cholestasis [PFIC].