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Fibrosis clinical trials

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NCT ID: NCT02181452 Completed - Liver Fibrosis Clinical Trials

Liver Fibrosis Assessment With ShearWave Elastography

Start date: November 2013
Phase: N/A
Study type: Observational

Chronic liver disease/fibrosis can be the result of various causes, and the result is that the liver tissue becomes stiff. ShearWave™ elastography, available on the Aixplorer® ultrasound system, is a method that can be used to measure the stiffness of organs in the body, for example the liver. This study will evaluate how this technology performs as a non-invasive test to stage liver fibrosis in patients with chronic liver disease.

NCT ID: NCT02179710 Completed - Cystic Fibrosis Clinical Trials

Cystic Fibrosis Treatment Adherence Cayston Proof-of-Concept Pilot Study

Start date: March 2015
Phase: N/A
Study type: Observational

Real-world adherence to inhaled and oral therapies for cystic fibrosis (CF) patients remains discouragingly low, ranging between 31-53% for inhaled antibiotics and 41-72% for hypertonic saline. Programs to enhance adherence, including comprehensive behavioral interventions with adolescents, have met with mixed success. Advances in therapy, treatment delivery systems, and data capture technology offer the potential for enhancing adherence by providing immediate and more frequent feedback to the patient regarding his or her fidelity to the prescribed treatment regimen. We propose to conduct a proof-of-concept study to evaluate a systematic approach to linking treatment and feedback components to enhance adherence.

NCT ID: NCT02173288 Completed - Cirrhosis Clinical Trials

Role of Midodrine and Tolvaptan in Patients With Cirrhosis With Refractory or Recurrent Ascites

Start date: July 2013
Phase: Phase 2/Phase 3
Study type: Interventional

The development of ascites in the natural history of cirrhosis heralds a worsening of the prognosis to 50% survival at 2 years, and this deteriorates to 30-50% at 1 year when the ascites becomes refractory to medical therapy. Hemodynamic alterations and their relation to neurohumoral systems are essential in pathophysiology of ascites formation. The theory that best explain the ascites formation and sodium retention in cirrhotics is portal hypertension leading to splanchnic arterial vasodilatation leading to underfilling of arterial circulation which is sensed by the arterial and the cardiopulmonary receptors leading to sympathetic nervous system activation and activation of the anti-natriuretic factors (RAAS and arginine vasopressin), resulting in sodium and water retention. The therapeutic options available for patients with refractory ascites are serial therapeutic paracentesis, liver transplantation and transjugular intrahepatic portosystemic shunts.Vasopressin V2 receptor antagonists antagonize the antidiuretic effects of vasopressin at the V2 receptor located in the renal collecting duct, they increase free water clearance, and thus may be helpful in mobilizing excess water in conditions associated with water retention including cirrhosis. The use of V2 receptor antagonists in cirrhosis with ascites has been shown to be safe and efficacious. Midodrine, an alpha adreno receptor agonist by causing splanchnic vasoconstriction has been used in hepatorenal syndrome (HRS) and for control of ascites in patients with refractory or recurrent ascites. It is possible that vasoconstrictors and aquaretics (V2 receptor antagonists) by acting at different sites in combination may reverse some of the pathogenic events that results in refractory or recurrent ascites.There are no reports on the use of combination of midodrine and tolvaptan in the patients with cirrhosis with ascites. Therefore, we plan to study the role of midodrine, tolvaptan and their combination on systemic hemodynamics, renal functions and control of ascites in patients with cirrhosis and refractory or recurrent ascites.

NCT ID: NCT02173145 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

Azithromycin in Idiopathic Pulmonary Fibrosis

Start date: August 19, 2014
Phase: N/A
Study type: Interventional

Idiopathic pulmonary fibrosis (IPF) is a devastating disease with no cure available. Patients suffer from respiratory symptoms including dyspnea and cough. To improve life quality the investigators will test the effects of immunomodulation of macrolides specifically on cough in IPF patients. The investigators hypothesize that immunomodulatory treatment reduces cough frequency and might improve lung function.

NCT ID: NCT02172534 Completed - Cystic Fibrosis Clinical Trials

Safety, Tolerability and Pharmacokinetics of Tiotropium in Cystic Fibrosis Patients

Start date: September 2006
Phase: Phase 1
Study type: Interventional

Study to obtain information about the safety and tolerability of tiotropium bromide administered via the Respimat® inhalation device in pediatric (≤11 y.o.) and adolescent/adult (≥12 y.o.) cystic fibrosis (CF) patients after single and multiple doses as well as to obtain pharmacokinetic data for tiotropium in CF patients after single and multiple doses

NCT ID: NCT02163512 Completed - Hepatic Cirrhosis Clinical Trials

Effect of Beta-adrenergic Blockers on Cardiac Function, Systemic and Splanchnic Haemodynamic and Kidney Function in Cirrhotic Patiets With Refractory Ascites

ALB-BET
Start date: March 12, 2014
Phase:
Study type: Observational

Multicentric, observational and prospective study with two groups of treatment: Refractory ascites and non-refractory ascites. All patients should be prescribed beta-adrenergic blockers as primary or secondary profilaxis for variceal bleeding.

NCT ID: NCT02161952 Completed - Fibrosis Clinical Trials

Pirfenidone, an Antifibrotic and Antiinflammatory Drug

Start date: May 2005
Phase: Phase 2
Study type: Interventional

The aim of this study was to assess whether two-year treatment with Pirfenidone influence necro-inflammation, fibrosis and steatosis in patients with chronic hepatitis C.

NCT ID: NCT02157922 Completed - Cystic Fibrosis Clinical Trials

A Phase IIb Study of OligoG in Subjects With Cystic Fibrosis

SMR-2984
Start date: October 2014
Phase: Phase 2
Study type: Interventional

The purpose of the study is assessment of efficacy and safety of OligoG as a dry powder formulation, in adult subjects with cystic fibrosis.

NCT ID: NCT02154282 Completed - Cirrhosis Clinical Trials

iPod Games in Hepatic Encephalopathy

Start date: January 2013
Phase: N/A
Study type: Interventional

To see if using ipod games can improve mental functioning

NCT ID: NCT02151864 Completed - Clinical trials for Hepatocellular Carcinoma

LDE225 in Patients With Advanced or Metastatic Hepatocellular Carcinoma and Child-Pugh A/B7 Cirrhosis

Start date: July 2014
Phase: Phase 1
Study type: Interventional

The purpose of this study is to test the safety and determine the maximum safe dose of an experimental drug called LDE225 (hedgehog inhibitor) in people with liver cancer. We have identified hedgehog dysregulation as a novel mechanism for hepatocarcinogenesis and hepatic fibrosis/cirrhosis. Therefore, we hypothesize that the hedgehog inhibitor may be an ideal drug target for treating both hepatocellular carcinoma (HCC) and Child-Pugh A cirrhosis (CPA).