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Cholangitis clinical trials

View clinical trials related to Cholangitis.

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NCT ID: NCT04370145 Completed - Clinical trials for Treatment Compliance

Antibiotics Treatment of Cholangitis Post-Kasai Portoenterostomy

Start date: May 1, 2021
Phase: Phase 4
Study type: Interventional

Application of multi-center, prospective study on the severity of postoperative cholangitis biliary atresia classification, according to the degree of cholangitis targeted therapy, to improve the therapeutic effect of postoperative cholangitis biliary atresia, decrease the overuse of antibiotics related complications.

NCT ID: NCT04309773 Recruiting - Clinical trials for Primary Sclerosing Cholangitis

Efficacy of 24 Month of Bezafibrate in Primary Sclerosing Cholangitis With Persistent Cholestasis Despite Ursodeoxycholic Acid Therapy

BEZASCLER
Start date: April 6, 2021
Phase: Phase 3
Study type: Interventional

The objectives of this study are to evaluate the effect of bezafibrate treatment compared to placebo on efficacy and safety in patients with primary sclerosing cholangitis (PSC) and persistent cholestasis despite ursodeoxycholic acid therapy

NCT ID: NCT04265235 Terminated - Clinical trials for Primary Biliary Cholangitis

EXerCise Intervention in cholesTatic LivEr Disease: The EXCITED Study

EXCITED
Start date: April 7, 2019
Phase: N/A
Study type: Interventional

A prospective, single centre, single-arm, pilot study investigating the safety and efficacy of a 12-week remotely-monitored home-based exercise program in patients with refractory fatigue (based on PBC-40 Quality of Life measure) secondary to Primary Biliary Cirrhosis.

NCT ID: NCT04216745 Recruiting - Cholangitis Clinical Trials

Microbial Analysis in Patients With Cholangitis

Start date: March 1, 2020
Phase:
Study type: Observational

- To identify the microbial profile in bile and blood for patients with cholangitis. - To explore risk factors of cholangitis and outcomes in those patients

NCT ID: NCT04181138 Recruiting - Liver Diseases Clinical Trials

Primary Sclerosing Cholangitis in Children

Start date: December 30, 2021
Phase:
Study type: Observational

Primary sclerosing cholangitis (PSC) is a rare liver disease that damages the liver's bile ducts. Bile ducts are tiny tubes that carry bile from the liver to the small intestine. Bile is a liquid produced by the liver that helps us absorb and use the nutrients in the food we eat. In people with PSC, the bile backs up into the liver and will damage it, causing scarring of the liver. The purposes of this study are to: - Collect medical and other data to learn more about PSC, how it progresses, and identify factors that may cause the disease to progress more quickly. - Ask questions about how PSC symptoms affect your child's life to learn more about its impact on your child's daily functioning - Children with PSC who are seen at one of the participating clinical sites in the Childhood Liver Disease Research Network (ChiLDReN) will be asked to contribute information, DNA, and other specimens. The information and specimens will be available to investigators to carry out approved research aimed at learning more about the possible causes and long-term effects of PSC.

NCT ID: NCT04173286 Recruiting - Acute Cholangitis Clinical Trials

Is Short Antibiotherapy Duration After Drainage Suitable for Patients Admitted in Intensive Care Medicine With a Severe Acute Cholangitis?

CASCAD
Start date: October 7, 2019
Phase:
Study type: Observational

Acute cholangitis (AC) occurs when biliary stenosis, due to various benign causes (often gallstones) or the presence of a tumour, leads to cholestasis and biliary infection. AC is a life-threatening infection if not diagnosed and treated in time, its mortality ranges from 1.4% to 5.2%. AC can be classified into different stages of severity depending on organ failure. A severity classification has been proposed by the Asian recommendations of Tokyo 2013: Grade I (Benin), Grade II (Moderate) and Grade III (Severe). AC treatment includes endoscopic or percutaneous bile drainage in combination with systemic antibiotic treatment. It is currently recommended that patients with severe CA (Grade III) have biliary drainage within 24 hours, although it has not been shown to improve their survival. The emergence of antibiotic-resistant germs, which is a public health issue, calls for reasonable and considered use of antibiotics. Reducing the duration of antibiotic therapy is a fundamental measure of antimicrobial management and antibiotics sparing. 7 to 10 days of antibiotic treatment is common in the treatment of CA. A 14-day treatment is recommended in case of associated bacteremia. A recent study of 263 patients showed that reducing the duration of antibiotic therapy to less than 7 days in patients with CA associated with bacteremia with effective drainage does not increase the risk of recurrence or mortality at 30 days. However, this study was monocentric retrospective and compared groups that were unbalanced in terms of CA severity. The optimal duration of antibiotic therapy in the treatment of CA in critically ill patients hospitalized in intensive care remains poorly known. The main purpose of this study is to compare short antibiotic therapy with long antibiotic therapy in terms of mortality in patients with AC admitted in intensive care unit (ICU).

NCT ID: NCT04133792 Recruiting - Clinical trials for Primary Sclerosing Cholangitis

Effect of Simvastatin on the Prognosis of Primary Primary Sclerosing Cholangitis (PSC)

PiSCATIN
Start date: October 1, 2020
Phase: Phase 3
Study type: Interventional

This is a randomized, double-blind, placebo controlled multicenter study. A total of 700 patients will be included. The study will include patients with primary sclerosing cholangitis (PSC) for daily intake of 40 mg simvastatin/placebo for 5 years. The aim is to study effect of prognosis of PSC by long term intake of simvastatin. Outcome measures are death, liver transplantation, cholangiocarcinoma or bleeding from esophageal varices. Subjects will be randomized (1:1) between Simvastatin and placebo.

NCT ID: NCT04076527 Recruiting - Clinical trials for Primary Biliary Cholangitis

Prospective, Multicenter Cohort Study on Primary Biliary Cholangitis

PBC-Cohort
Start date: September 19, 2019
Phase:
Study type: Observational

The German PBC Cohort is a multi-centric, observational (non-interventional) study with three parallel groups. The main objective of this observational study is to describe the course of Primary biliary cholangitis (PBC) in patients in Germany under routine treatment with approved drugs. Therefore, the effectiveness and safety/tolerability of PBC treatment options in a real-life setting will be evaluated.

NCT ID: NCT04060147 Terminated - Clinical trials for Primary Sclerosing Cholangitis

Safety and Tolerability of Cilofexor in Participants With Primary Sclerosing Cholangitis (PSC) and Compensated Cirrhosis

Start date: October 17, 2019
Phase: Phase 1
Study type: Interventional

The primary objective of this study is to assess the safety and tolerability of escalating doses of cilofexor (CILO) in participants with primary sclerosing cholangitis (PSC) and compensated cirrhosis.

NCT ID: NCT04047160 Completed - Clinical trials for Liver Cirrhosis, Biliary

Safety, Tolerability of OP-724 in Patients With Primary Biliary Cholangitis (Phase I)

Start date: August 29, 2019
Phase: Phase 1
Study type: Interventional

To evaluate the safety and pharmacokinetics of OP-724 and to determine the recommended dose of OP-724 against Primary Biliary Cholangitis patients.