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Fibrosis clinical trials

View clinical trials related to Fibrosis.

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NCT ID: NCT01266473 Completed - Cystic Fibrosis Clinical Trials

Study of Individualized Physiotherapy for Airway Clearance in Cystic Fibrosis.

Start date: August 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate individual efficacy in Physiotherapy for Airway Clearance, and to investigate user experience, i.e.utility value and preference.

NCT ID: NCT01265888 Completed - Clinical trials for Pulmonary Arterial Hypertension

Study in Subjects With PAH and PH Secondary to IPF Using Inhaled GeNOsyl.

PHiano
Start date: March 2011
Phase: Phase 2
Study type: Interventional

A Phase 2 open label, dose escalation study to find the minimally and maximum effective dose (dose beyond which no further effect on PVR is seen) of inhaled nitric oxide generated by the GeNOsyl® System compared to placebo.

NCT ID: NCT01265173 Completed - Liver Cirrhosis Clinical Trials

Comparison of Efficacy of Cefotaxime, Ceftriaxone, and Ciprofloxacin for the Treatment of SBP in Patients With LC

Start date: April 2007
Phase: Phase 4
Study type: Interventional

Spontaneous bacterial peritonitis (SBP) is one of the most serious complications of liver cirrhosis. Mainstay of treatment for SBP is use of proper antibiotics. Although, several antibiotics including cefotaxime, ceftriaxone, or ciprofloxacin are being used, it is unclear which drug is most effective. Our aim of study is to compare the efficacy of the three current antibiotics for the treatment of SBP in patients with liver cirrhosis. The primary hypothesis is that the efficacy of all the antibiotics will not significantly different. This is non-inferiority trial.

NCT ID: NCT01262352 Completed - Cystic Fibrosis Clinical Trials

Study of the Effect of Ivacaftor on Lung Clearance Index in Subjects With Cystic Fibrosis and the G551D Mutation

Start date: January 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effect of ivacaftor (VX-770) on lung clearance index (LCI) in subjects aged 6 years and older with cystic fibrosis (CF) who have the G551D-CFTR mutation on at least 1 allele.

NCT ID: NCT01262001 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

Safety, Tolerability, and Efficacy Study of Idiopathic Pulmonary Fibrosis

FGCL-3019-049
Start date: March 2011
Phase: Phase 2
Study type: Interventional

To evaluate the safety and tolerability of FG-3019 in subjects with Idiopathic Pulmonary Fibrosis (IPF) and the efficacy of FG-3019 for attenuating fibrosis in these subjects.

NCT ID: NCT01254409 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

A Phase 1b Study of IV PRM151 in Patients With Idiopathic Pulmonary Fibrosis (IPF)

PRM151F-12GL
Start date: March 29, 2011
Phase: Phase 1
Study type: Interventional

The aims of the study are to assess safety, tolerability, the pharmacokinetic profile, and the pharmacodynamic profile of multiple doses of PRM-151 administered IV to IPF patients.

NCT ID: NCT01241227 Completed - Liver Fibrosis Clinical Trials

Prognosis Value of Transient Elastography and Non-invasive Markers of Fibrosis in Patients With Chronic Liver Disease

PVTE
Start date: April 2003
Phase:
Study type: Observational

The aim of this prospective study was to compare the 5-year prognostic value of transient elastography (TE), FibroTest (FT), APRI , FIB-4, Lok, and Child-Pugh scores for predicting survival and complications of cirrhosis in patients with chronic liver diseases.

NCT ID: NCT01238081 Completed - Cystic Fibrosis Clinical Trials

The Role of Respiratory Viruses in Exacerbations of Cystic Fibrosis in Adults

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

Respiratory viruses, such as those that cause colds and influenza, are very common in the general population. The average adult will experience between 2 and 4 viral respiratory illnesses each year. It is known that respiratory viruses can cause flare-ups of chronic lung diseases such as asthma and chronic obstructive pulmonary disease. In children with CF, respiratory viral infections have been identified in nearly half of all exacerbations and are associated with a decline in lung function and increased frequency of hospital admission and acquisition of new bacterial pathogens. Currently, little is known about the impact of viral infections on the course of CF lung disease in adults and no large-scale prospective studies in this area have been performed to date. It is unknown how often respiratory viruses can be found in patients with CF when they are well and what consequences they have on the course of exacerbations of CF lung disease. This study will identify the frequency of common viral infections in adults with CF and determine the effects they have on lung function, the rate and diversity of bacterial infection and patients' treatment burden. The information gained from this study will lead to improved prevention and treatment of respiratory infections in CF.

NCT ID: NCT01232478 Completed - Cystic Fibrosis Clinical Trials

I Change Adherence & Raise Expectations

iCARE
Start date: October 2009
Phase: Phase 3
Study type: Interventional

The iCARE study, a clustered-randomized controlled trial, is evaluating an adherence promotion intervention for adolescents that Cystic Fibrosis (CF) care teams will implement. Half the centers will receive the Comprehensive Adherence Program (CAP) for 2 years. CAP consists of training in the CF My Way program (a validated problem-solving adherence promotion intervention). The other half of the centers will receive CAP in year 2 of the study. Participants are patients age 11-20 years old who are diagnosed with CF and have been prescribed at least one of the following medications for at least 6 months prior to signing the informed consent: azithromycin, hypertonic saline, Pulmozyme®, TOBI®, or inhaled compounded tobramycin. Rate of refilling prescriptions is the primary outcome with lung function decline rates, exacerbation rates, and patient reported measures including health related quality of life and CF knowledge and skills, as secondary outcomes. A central goal of this study is to test the effectiveness of the comprehensive adherence program (CAP), described above, versus standard care (SC) for adolescents and young adults seen in outpatient CF clinics.

NCT ID: NCT01231685 Completed - HIV Clinical Trials

Raltegravir Switch Study to Reduce Liver Fibrosis Progression in HIV-Hepatitis C Co-infection

Start date: December 2011
Phase: Phase 2
Study type: Interventional

HIV infection exerts a negative impact on the course of HCV infection. Co-infected individuals progress more rapidly to liver fibrosis, cirrhosis and ESLD compared to those infected with HCV alone. Some of the this accelerated fibrosis may be related to longterm chronic toxicity from protease inhibitor based ART. Hypothesis: Switching from ritonavir boosted-PI based ART regimen to a Raltegravir-based regimen will reduce the rate of hepatic fibrosis progression in HIV-HCV co-infected patients as measured by transient elastography (Fibroscan®) and the AST-to-platelet ratio index (APRI).